Methods for treating carbonate hydrocarbon-bearing formations with fluorinated amphoteric compounds

Method of treating a carbonate hydrocarbon-bearing formation. The method includes contacting the hydrocarbon-bearing formation with a composition comprising solvent and a fluorinated amphoteric compound. Carbonate hydrocarbon-bearing formations treated according to the method are also disclosed.

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Description
CROSS-REFERENCE TO RELATED APPLICATION

This application is a national stage filing under 35 U.S.C. 371 of PCT/US2010/040870, filed Jul. 2, 2010, which claims priority to U.S. Provisional Application No. 61/224,250, filed Jul. 9, 2009, the disclosure of which is incorporated by reference herein in its entirety.

BACKGROUND

In the oil and gas industry, certain surfactants (including certain fluorinated surfactants) are known as fluid additives for various downhole operations (e.g., fracturing, waterflooding, and drilling). Often, these surfactants function to decrease the surface tension of the fluid or to stabilize foamed fluids.

Some hydrocarbon and fluorochemical compounds have been used to modify the wettability of reservoir rock, which may be useful, for example, to prevent or remedy water blocking (e.g., in oil or gas wells) or liquid hydrocarbon accumulation (e.g., in gas wells) in the vicinity of the wellbore (i.e., the near wellbore region). Water blocking and liquid hydrocarbon accumulation may result from natural phenomena (e.g., water-bearing geological zones or condensate banking) and/or operations conducted on the well (e.g., using aqueous or hydrocarbon fluids). Water blocking and condensate banking in the near wellbore region of a hydrocarbon-bearing geological formation can inhibit or stop production of hydrocarbons from the well and hence are typically not desirable. Not all hydrocarbon and fluorochemical compounds, however, provide the desired wettability modification. And some of these compounds modify the wettability of siliciclastic hydrocarbon-bearing formations but not carbonate formations, or vice versa. Hence, there is a continuing need for alternative and/or improved techniques for increasing the productivity of oil and/or gas wells that have brine and/or two phases of hydrocarbons in a near wellbore region of a hydrocarbon-bearing geological formation.

SUMMARY

The methods described herein may be useful in hydrocarbon-bearing formations having at least one of brine (e.g., connate brine and/or water blocking) or two phases of hydrocarbons present in the near wellbore region, (e.g., in gas wells having retrograde condensate and oil wells having black oil or volatile oil), resulting in an increase in permeability of at least one of gas, oil, or condensate. Treatment of an oil and/or gas well that has brine and/or two phases of hydrocarbons in the near wellbore region using the methods disclosed herein may increase the productivity of the well. Although not wishing to be bound by theory, it is believed that the fluorinated amphoteric compounds disclosed herein generally at least one of adsorb to, chemisorb onto, or react with carbonate hydrocarbon-bearing formations under downhole conditions and modify the wetting properties of the rock in the formation to facilitate the removal of hydrocarbons and/or brine.

To optimize efficiency and minimize cost, it is typically desirable to use the lowest effective concentration of a fluorochemical for modifying the wetting properties of the rock in a hydrocarbon-bearing formation. The methods described herein have been found to be surprisingly effective when the fluorinated amphoteric compound is present at up to 1 percent by weight, based on the total weight of the treatment composition.

In one aspect, the present disclosure provides a method of treating a hydrocarbon-bearing formation, the method comprising:

contacting the hydrocarbon-bearing formation with a treatment composition comprising solvent and a fluorinated amphoteric compound, wherein the hydrocarbon-bearing formation comprises carbonate, and wherein the fluorinated amphoteric compound is selected from the group consisting of:

    • (a)

    • (b) Rf-Q-Z
    • (c) a compound comprising:
      • a first divalent unit represented by

      • and
      • a second divalent unit represented by formula


and

    • (d) combinations thereof;
      wherein

Rf is independently fluoroalkyl having up to 10 carbon atoms or a polyfluoropolyether group;

each Rf1 is independently fluoroalkyl having up to 10 carbon atoms or a polyfluoropolyether group;

X is —SO2— or —C(O)—;

Y is —N(R)2, —N+(R)3, or —N+(R)3A-, wherein A- is a counter anion;

Y′ is —P(O)(OM)2, —O—P(O)(OM)2, —SO3M, —O—SO3M, or —CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation;

each Q is independently —SO2—N(R′)—W—, —C(O)—N(R′)—W—, alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O—, —S—, —SO2— or —C(O)—;

each W is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl;

Z is —N+(R)2—V—SO3M, or —N+(R)2—V—CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation;

each V is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl;

each R is independently hydrogen, alkyl, or aryl, wherein alkyl may optionally be interrupted by —O— or substituted with hydroxyl or aryl, or two R groups taken together with the N atom to which they are attached can form a heterocyclic ring having up to six carbon atoms and optionally containing —O— or —S—;

R′ is hydrogen, alkyl having up to 6 carbon atoms, or aryl;

each R1 is independently hydrogen or methyl; and

each Q1 is independently —O—, —S—, or —N(R″)—, wherein R″ is hydrogen or alkyl having up to 6 carbon atoms.

In another aspect, the present disclosure provides a hydrocarbon-bearing formation treated according to the method disclosed herein.

Hydrocarbon-bearing formations that comprise carbonate include limestone or dolomite formations, wherein limestone or dolomite forms at least a portion (e.g., at least 50, 60, 75, or 90 percent by weight) of the formation. In some embodiments of the foregoing aspects, the hydrocarbon-bearing formation comprises limestone (e.g., at least 50, 60, 75, or 90 percent by weight limestone).

In some embodiments of the foregoing aspects, the fluorinated amphoteric compound is represented by formula:


wherein Rf is perfluoroalkyl having up to 6 carbon atoms, wherein each W is independently alkylene having up to 4 carbon atoms, and wherein Y′ is —SO3M, or —CO2M. In some embodiments, the fluorinated amphoteric compound is represented by formula Rf-Q-Z, wherein Rf is perfluoroalkyl having up to 6 carbon atoms, Q is —SO2—N(R′)—W— or alkylene having up to four carbon atoms, wherein R′ is hydrogen or alkyl having up to four carbon atoms, and wherein W is alkylene having up to 4 carbon atoms. In some embodiments, the fluorinated amphoteric compound is the compound comprising:

    • the first divalent unit represented by


and

    • the second divalent unit represented by formula


wherein Rf1 is perfluoroalkyl having up to 6 carbon atoms; Q is —SO2—N(R′)—W— or alkylene having up to four carbon atoms, wherein R′ is hydrogen or alkyl having up to four carbon atoms, and wherein W and V are each independently alkylene having up to four carbon atoms.

In some embodiments of the foregoing aspects, the solvent comprises at least one of water, a monohydroxy alcohol, an ether, a ketone, a glycol, a glycol ether, or supercritical carbon dioxide.

In some embodiments of the foregoing methods, the hydrocarbon-bearing formation is a gas producing formation penetrated by a wellbore, and a region near the wellbore is contacted with the treatment composition. In some of these embodiments, the method further comprises obtaining gas from the wellbore after contacting the hydrocarbon-bearing formation with the composition. The region near the wellbore (i.e., near wellbore region) includes a region within about 25 feet (in some embodiments, 20, 15, or 10 feet) of the wellbore. In some embodiments, before contacting the hydrocarbon-bearing formation with the treatment composition, the hydrocarbon-bearing formation has retrograde gas condensate, black oil, or volatile oil, and the hydrocarbon-bearing formation has an increase in at least gas permeability after it is contacted with the treatment composition.

In this application:

Terms such as “a”, “an” and “the” are not intended to refer to only a singular entity, but include the general class of which a specific example may be used for illustration. The terms “a”, “an”, and “the” are used interchangeably with the term “at least one”.

The phrase “at least one of” followed by a list refers to any one of the items in the list and any combination of two or more items in the list.

The term “brine” refers to water having at least one dissolved electrolyte salt therein (e.g., sodium chloride, calcium chloride, strontium chloride, magnesium chloride, potassium chloride, ferric chloride, ferrous chloride, and hydrates thereof) at any nonzero concentration (in some embodiments, less than 1000 parts per million by weight (ppm), or greater than 1000 ppm, greater than 10,000 ppm, greater than 20,000 ppm, 30,000 ppm, 40,000 ppm, 50,000 ppm, 100,000 ppm, 150,000 ppm, or even greater than 200,000 ppm).

The term “hydrocarbon-bearing formation” includes both hydrocarbon-bearing formations in the field (i.e., subterranean hydrocarbon-bearing formations) and portions of such hydrocarbon-bearing formations (e.g., core samples).

The term “productivity” as applied to a well refers to the capacity of a well to produce hydrocarbons (i.e., the ratio of the hydrocarbon flow rate to the pressure drop, where the pressure drop is the difference between the average reservoir pressure and the flowing bottom hole well pressure (i.e., flow per unit of driving force)).

The term “contacting” includes placing a composition within a hydrocarbon-bearing formation using any suitable manner known in the art (e.g., pumping, injecting, pouring, releasing, displacing, spotting, or circulating the treatment composition into a well, wellbore, or hydrocarbon-bearing formation).

“Alkyl group” and the prefix “alk-” are inclusive of both straight chain and branched chain groups and of cyclic groups. Unless otherwise specified, alkyl groups herein have up to 20 carbon atoms. Cyclic groups can be monocyclic or polycyclic and, in some embodiments, have from 3 to 10 ring carbon atoms. “Alkylene” is the divalent form of “alkyl”.

The term “fluoroalkyl” includes linear, branched, and/or cyclic alkyl groups in which all C—H bonds are replaced by C—F bonds as well as groups in which hydrogen or chlorine atoms are present instead of fluorine atoms provided that up to one atom of either hydrogen or chlorine is present for every two carbon atoms. In some embodiments of fluoroalkyl groups, when at least one hydrogen or chlorine is present, the fluoroalkyl group includes at least one trifluoromethyl group. The term “perfluoroalkyl group” includes linear, branched, and/or cyclic alkyl groups in which all C—H bonds are replaced by C—F bonds. The term “interrupted by up to 5 ether groups” refers to having fluoroalkyl on both sides of the ether group.

The term “aryl” as used herein includes carbocyclic aromatic rings or ring systems, for example, having 1, 2, or 3 rings, optionally containing at least one heteroatom (e.g., O, S, or N) in the ring, and optionally substituted by up to five substituents including one or more alkyl groups having up to 4 carbon atoms (e.g., methyl or ethyl), alkoxy having up to 4 carbon atoms, halo (i.e., fluoro, chloro, bromo or iodo), hydroxy, or nitro groups. Examples of aryl groups include phenyl, naphthyl, biphenyl, fluorenyl as well as furyl, thienyl, oxazolyl, and thiazolyl.

“Arylene” is the divalent form of the “aryl” groups defined above.

“Alkylarylene” refers to an “arylene” moiety to which an alkyl group is attached.

“Arylalkylene” refers to an “alkylene” moiety to which an aryl group is attached.

The term “solvent” refers to a homogeneous liquid material, which may be a single compound or a combination of compounds and which may or may not include water, that is capable of at least partially dissolving a fluorinated amphoteric compound disclosed herein at 25° C.

The term “polymer” refers to a molecule having a structure which essentially includes the multiple repetition of units derived, actually or conceptually, from molecules of low relative molecular mass. The term “polymer” encompasses oligomers. Polymers may have repeating units from the same monomer or a combination of monomers.

The term “precipitate” means to separate from solution and remain separated under the conditions of the treatment method (e.g., in the presence of the brine and at the temperature of the hydrocarbon-bearing formation).

All numerical ranges are inclusive of their endpoints and non-integral values between the endpoints unless otherwise stated.

BRIEF DESCRIPTION OF THE DRAWINGS

For a more complete understanding of the features and advantages of the present disclosure, reference is now made to the detailed description along with the accompanying figures and in which:

FIG. 1 is a schematic illustration of an exemplary embodiment of an offshore oil platform operating an apparatus for progressively treating a near wellbore region according to the present disclosure;

FIG. 2 is a schematic illustration of the flow apparatus used for Examples 1 to 5 and Comparative Example A; and

FIG. 3 is a schematic illustration of a core flood set-up that can be used to evaluate the method disclosed herein in a laboratory.

 DETAILED DESCRIPTION

Methods according to the present disclosure include contacting a hydrocarbon-bearing formation with a composition comprising solvent and a fluorinated amphoteric compound. In some embodiments, the fluorinated amphoteric compound is represented by formula:


Rf-Q-Z, or combinations thereof. In some embodiments, the fluorinated amphoteric compound is represented by formula:


In some embodiments, the fluorinated amphoteric compound is represented by formula Rf-Q-Z. In some embodiments, the fluorinated amphoteric compound is the compound comprising:

    • at least one (e.g., at least 2, 5, or 10, for example in a range from 1 to 100 or 1 to 20) first divalent unit represented by formula


and

    • at least one (e.g., at least 2, 5, or 10, for example in a range from 1 to 100 or 1 to 20) second divalent unit represented by formula

In any of the above embodiments having an Rf group, Rf may be a fluoroalkyl group having up to 10 carbon atoms (e.g., up to 8, 6, or 4 carbon atoms, for example, in a range from 2 to 10, 4 to 8, or 2 to 6 carbon atoms). Rf may be a mixture of fluoroalkyl groups.

In some embodiments, Rf is a polyfluoropolyether group. The term “polyfluoropolyether” refers to a compound or group having at least 3 (in some embodiments, at least 4, 5, 6, 7, 8, 9, 10, 11, 12, 13, 14, 15, 16, 17, 18, 19, or even 20) carbon atoms and at least 3 (in some embodiments, at least 4, 5, 6, 7, or even 8) ether linkages, wherein the hydrogen atoms on the carbon atoms are replaced with fluorine atoms. In some embodiments, Rf has up to 100, 110, 120, 130, 140, 150, or even 160 carbon atoms and up to 25, 30, 35, 40, 45, 50, 55, or even 60 ether linkages.

The polyfluoropolyether group Rf can be linear, branched, cyclic, or combinations thereof and can be saturated or unsaturated. Polyfluoropolyether groups include those in which hydrogen or chlorine atoms are present instead of fluorine atoms provided that up to one atom of either hydrogen or chlorine is present for every two carbon atoms. In some embodiments, the polyfluoropolyether group is a perfluoropolyether group (i.e., all of the hydrogen atoms on the carbon atoms are replaced with fluorine atoms). Exemplary perfluoropolyethers include perfluorinated repeating units represented by at least one of —(CdF2d)—, —(CdF2dO)—, —(CF(L′))-, —(CF(L′)O)—, —CF(L′)CdF2dO)—, —(CdF2dCF(L′)O)—, or —(CF2CF(L′)O)—. In these repeating units, d is typically an integer of 1 to 10. In some embodiments, d is an integer of 1 to 8, 1 to 6, 1 to 4, or 1 to 3. The L′ group can be a perfluoroalkyl group optionally interrupted by at least one ether linkage or a perfluoroalkoxy group, each of which may be linear, branched, cyclic, or a combination thereof. The L′ group typically has up to 12 (in some embodiments, up to 10, 8, 6, 4, 3, 2, or 1) carbon atoms. In some embodiments, the L′ group can have up to 4 (in some embodiments, up to 3, 2, or 1) oxygen atoms; in some embodiments L′ has no oxygen atoms. In these perfluoropolyether structures, different repeating units can be combined in a block or random arrangement to form the Rf group. Rf may be a mixture of polyfluoropolyether groups.

In some embodiments, Rf is represented by formula Rfa—O—(Rfb—O—)z′(Rfc)—, wherein Rfa is a perfluoroalkyl having 1 to 10 (in some embodiments, 1 to 6, 1 to 4, 2 to 4, or 3) carbon atoms; each Rfb is independently a perfluoroalkylene having 1 to 4 (i.e., 1, 2, 3, or 4) carbon atoms; Rfc is a perfluoroalkylene having 1 to 6 (in some embodiments, 1 to 4 or 2 to 4) carbon atoms; and z′ is in a range from 2 to 50 (in some embodiments, 2 to 25, 2 to 20, 3 to 20, 3 to 15, 5 to 15, 6 to 10, or 6 to 8). Representative Rfa groups include CF3—, CF3CF2—, CF3CF2CF2—, CF3CF(CF3)—, CF3CF(CF3)CF2—, CF3CF2CF2CF2—, CF3CF2CF(CF3)—, CF3CF2CF(CF3)CF2—, and CF3CF(CF3)CF2CF2—. In some embodiments, Rfa is CF3CF2CF2—. Representative Rfb groups include —CF2—, —CF(CF3)—, —CF2CF2—, —CF(CF3)CF2—, —CF2CF2CF2—, —CF(CF3)CF2CF2—, —CF2CF2CF2CF2—, and —CF2C(CF3)2—. Representative Rfc groups include —CF2—, —CF(CF3)—, —CF2CF2—, —CF2CF2CF2—, and —CF(CF3)CF2—. In some embodiments, Rfc is —CF(CF3)—.

In some embodiments, (Rfb—O—)z′, is represented by —[CF2O]i[CF2CF2O]j—, —[CF2O]i[CF(CF3)CF2O]j—, —[CF2O]i[CF2CF2CF2O]j—, —[CF2CF2O]i[CF2O]j—, —[CF2CF2O]i[CF(CF3)CF2O]j—, —[CF2CF2O]i[CF2CF2CF2O]j—, —[CF2CF2CF2O]i[CF2CF(CF3)O]j—, and [CF2CF2CF2O]i[CF(CF3)CF2O]j—, wherein i+j is an integer of at least 3 (in some embodiments, at least 4, 5, or 6).

In some embodiments, Rf is selected from the group consisting of C3F7O(CF(CF3)CF2O)xCF(CF3)—, C3F7O(CF2CF2CF2O)xCF2CF2—, or CF3O(C2F4O)yCF2—, wherein x has an average value in a range from 3 to 50 (in some embodiments, 3 to 25, 3 to 15, 3 to 10, 4 to 10, or 4 to 7), and wherein y has an average value in a range from 6 to 50 (in some embodiments, 6 to 25, 6 to 15, 6 to 10, 7 to 10, or 8 to 10). In some of these embodiments, Rf is C3F7O(CF(CF3)CF2O)kCF(CF3)—, wherein x has an average value in a range from 4 to 7. In some embodiments, Rf is selected from the group consisting of CF3O(CF2O)x′(C2F4O)y′CF2— and F(CF2)3—O—(C4F8O)z″(CF2)3—, wherein x′, y′, and z″ each independently has an average value in a range from 3 to 50 (in some embodiments, 3 to 25, 3 to 15, 3 to 10, or even 4 to 10).

In some embodiments, Rf has a weight average molecular weight of at least 750 (in some embodiments at least 850 or even 1000) grams per mole. In some embodiments, Rf has a weight average molecular weight of up to 6000 (in some embodiments, 5000 or even 4000) grams per mole. In some embodiments, Rf has a weight average molecular weight in a range from 750 grams per mole to 5000 grams per mole. Weight average molecular weights can be measured, for example, by gel permeation chromatography (i.e., size exclusion chromatography) using techniques known in the art.

In some embodiments, Rf is selected from the group consisting of:
Rfd—(O)r—CHF—(CF2)n—;
[Rfe—(O)t—C(L)H—CF2—O]m—W′—;
CF3CFH—O—(CF2)p—;
CF3—(O—CF2)z—; and
CF3—O—(CF2)3—O—CF2—;
wherein

    • Rfd and Rfe independently represent a partially or fully fluorinated alkyl group having from 1 to 10 carbon atoms and optionally interrupted with at least one oxygen atom;
    • L is selected from the group consisting of F and CF3;
    • W′ is selected from the group consisting of alkylene and arylene;
    • r is 0 or 1, wherein when r is 0, then Rfd is interrupted with at least one oxygen atom;
    • t is 0 or 1;
    • m is 1, 2, or 3;
    • n is 0 or 1;
    • each p is independently a number from 1 to 6; and
    • z is a number from 2 to 7.
      In some of these embodiments, Rf has a molecular weight of up to 600 grams per mole (in some embodiments, up to 500, 400, or even up to 300 grams per mole).
      Rfd and Rfe independently represent a partially or fully fluorinated alkyl group having from 1 to 10 carbon atoms and optionally interrupted with at least one oxygen atom. Rfd and Rfe include linear and branched alkyl groups. In some embodiments, Rfd and/or Rfe is linear. In some embodiments, Rfd and Rfe independently represent a fully fluorinated alkyl group having up to 6 (in some embodiments, 5, 4, 3, 2, or 1) carbon atoms. In some embodiments, Rfd and Rfe independently represent a fully fluorinated alkyl group interrupted with at least one oxygen atom, of which the alkyl groups between oxygen atoms have up to 6 (in some embodiments, 5, 4, 3, 2, or 1) carbon atoms, and wherein the terminal alkyl group has up to 6 (in some embodiments, 5, 4, 3, 2, or 1) carbon atoms. In some embodiments, Rfd and Rfe independently represent a partially fluorinated alkyl group having up to 6 (in some embodiments, 5, 4, 3, 2, or 1) carbon atoms and up to 2 hydrogen atoms. In some embodiments, Rfd and Rfe independently represent a partially fluorinated alkyl group having up 2 hydrogen atoms interrupted with at least one oxygen atom, of which the alkyl groups between oxygen atoms have up to 6 (in some embodiments, 5, 4, 3, 2, or 1) carbon atoms, and wherein the terminal alkyl group has up to 6 (in some embodiments, 5, 4, 3, 2, or 1) carbon atoms.

In some embodiments of Rf, Rfd and Rfe are independently represented by formula
Rf1—[ORf2]a—[ORf3]b—.
Rf1 is a perfluorinated alkyl group having from 1 to 6 (in some embodiments, 1 to 4) carbon atoms. Rf2 and Rf3 are each independently perfluorinated alkylene having from 1 to 4 carbon atoms. “a” and b are each independently a number having a value from 0 to 4, and the sum of “a” and b is at least 1. In some of these embodiments, t is 1, and r is 1.

In some embodiments of Rf, Rfd and Rfe are independently represented by formula
Rf4—[ORf5]a′—[ORf6]b′—O—CF2—.
Rf4 is a perfluorinated alkyl group having from 1 to 6 (in some embodiments, 1 to 4) carbon atoms. Rf5 and Rf6 are each independently perfluorinated alkylene having from 1 to 4 carbon atoms. a′ and b′ are each independently numbers having a value from 0 to 4. In some of these embodiments, t is 0, and r is 0.

In some embodiments of Rf, Rfd and Rfe are independently represented by formula Rf7—(OCF2)p—, wherein p is an integer of 1 to 6 (in some embodiments, 1 to 4), and Rf7 is selected from the group consisting of a partially fluorinated alkyl group having 1, 2, 3, 4, 5, or 6 carbon atoms and 1 or 2 hydrogen atoms and a fully fluorinated alkyl group having 1, 2, 3 or 4 carbon atoms.

In some embodiments of Rf, Rfd and Rfe are independently represented by formula Rf8—O—(CF2)p—, wherein p is a number from 1 to 6 (in some embodiments, 1 to 4) and Rf8 is selected from the group consisting of a partially fluorinated alkyl group having 1, 2, 3, 4, 5, or 6 carbon atoms and 1 or 2 hydrogen atoms and a fully fluorinated alkyl group having 1, 2, 3 or 4 carbon atoms.

In certain embodiments of Rf, L is selected from the group consisting of F and CF3. In some embodiments, L is F. In other embodiments, L is CF3.

In certain embodiments of Rf, W′ is selected from the group consisting of alkylene and arylene. Alkylene includes linear, branched, and cyclic alkylene groups having from 1 to 10 (in some embodiments, 1 to 4) carbon atoms. In some embodiments, W′ is methylene. In some embodiments, W′ is ethylene. Arylene includes groups having 1 or 2 aromatic rings, optionally having at least one heteroatom (e.g., N, O, and S) in the ring, and optionally substituted with at least one alkyl group or halogen atom. In some embodiments, W′ is phenylene.

In certain embodiments of Rf, t is 0 or 1. In some embodiments, t is 1. In some embodiments, t is 0. In embodiments wherein t is 0, Rfe is typically interrupted by at least one oxygen atom.

In certain embodiments of Rf, m is 1, 2, or 3. In some embodiments, m is 1.

In certain embodiments of Rf, n is 0 or 1. In some embodiments, n is 0. In some embodiments, n is 1.

In certain embodiments of Rf, p is a number from 1 to 6 (i.e., 1, 2, 3, 4, 5, or 6). In some embodiments, p is 1, 2, 5, or 6. In some embodiments, p is 3. In some embodiments, p is 1 or 2. In some embodiments, p is 5 or 6.

In certain embodiments of Rf, z is a number from 2 to 7 (i.e., 2, 3, 4, 5, 6, or 7). In some embodiments, z is an integer from 2 to 6, 2 to 5, 2 to 4, or 3 to 4.

In some embodiments, fluorinated amphoteric compounds disclosed herein have an Rf group represented by CF3CFH—O—(CF2)p—. In some of these embodiments Rf is selected from the group consisting of CF3CFH—O—(CF2)3— and CF3CFH—O—(CF2)5—.

In some embodiments, fluorinated amphoteric compounds disclosed herein have an Rf group represented by CF3—(O—CF2)z—. In some of these embodiments, z is a number from 2 to 6, 2 to 5, 2 to 4, 3 to 5, or 3 to 4.

In some embodiments, fluorinated amphoteric compounds disclosed herein have an Rf represented by CF3—O—(CF2)3—O—CF2—.

Other useful Rf structures include partially fluorinated Rf groups disclosed, for example, in PCT International Pub. No. WO 2008/154345 A1 (Dams et al.), pages 8 to 10, the disclosure of which is incorporated herein by reference.

For embodiments of fluorinated anionic compounds comprising first and second divalent units, each Rf1 is independently defined as in any of the embodiments of Rf above.

In any of the aforementioned embodiments containing an X group, X is —SO2— or —C(O)—. In some embodiments, X is —SO2—. In some embodiments, X is —C(O)—.

In any of the aforementioned embodiments containing a Y group, Y is —N(R)2, —N+(R)3, or —N+(R)3A-, wherein A- is a counter anion. Typical counter anions include halides (i.e., fluoride, chloride, bromide, and iodide), organic acid salts (e.g., formate, acetate, propionate, lactate, laurate, palmitate, stearate, or citrate), organic sulfonic or sulfuric acid salts (e.g., alkyl sulfates or alkanesulfonates), nitrate, and tetrafluoroborate. The organic acid salts and sulfonic acid salts may be partially fluorinated or perfluorinated. In some embodiments, A- is chloride, bromide, or iodide (i.e., Cl—, Br—, or I—). In some embodiments, A- is selected from the group consisting of chloride, acetate, iodide, bromide, methylsulfate, ethylsulfate, and formate.

In any of the aforementioned embodiments containing a Y′ group, Y′ is —P(O)(OM)2, —O—P(O)(OM)2, —SO3M, —O—SO3M, or —CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation. It should be understood that when M is a free anion, Y′ can also be written as —P(O)(O—)2, —O—P(O)(O—)2, —SO3—, —OSO3—, or —CO2—. In some embodiments, Y′ is —SO3M or —CO2M. Exemplary M counter cations include alkali metal (e.g., sodium, potassium, and lithium), alkaline earth metal (e.g., calcium and magnesium), and ammonium, alkyl ammonium (e.g., tetraalkylammonium). M may be a bond (e.g., an ionic bond, hydrogen bond, or covalent bond) to the hydrocarbon-bearing formation, for example, in embodiments of treated hydrocarbon-bearing formations disclosed herein.

It is generally understood that under neutral pH conditions (e.g., pH 6 to 8), Y typically is —N+(R)3, and M in Y′ is typically a free anion. Under strongly basic conditions (e.g., pH of at least 10), Y typically is —N(R)2, and M in Y′ is a counter cation. Under strongly acidic conditions (e.g, pH of up to 4), Y typically is —N+(R)3A-, and M in Y′ is hydrogen.

In any of the aforementioned embodiments containing an Q group, each Q is independently —SO2—N(R′)—W—, —C(O)—N(R′)—W—, alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O—, —S—, —SO2—, or —C(O)—; wherein R′ is hydrogen, an alkyl group having up to 6 carbon atoms, or aryl. The term “interrupted by —O—, —S—, —SO2—, or —C(O)—” refers to having a portion of the alkylene group on either side of the —O—, —S—, —SO2—, or —C(O)—. In some embodiments, Q is —SO2—N(R′)—W— or alkylene having up to four carbon atoms. In some embodiments, Q is —SO2—N(R′)—W—. In some embodiments, R′ is hydrogen or alkyl having up to four carbon atoms (e.g., methyl or ethyl). In some embodiments, Q is —CH2—CH2—.

In any of the aforementioned embodiments containing a W group, each W is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl. In some of these embodiments, W is alkylene (e.g., having up to 6, 4, or 3 carbon atoms).

In any of the aforementioned embodiments containing a Z group, Z is —N+(R)2—V—SO3M, or —N+(R)2—V—CO2M, wherein M can be defined as in any of the embodiments described above. In some embodiments, Z is —N+(R)2—V—SO3M. It is generally understood that under neutral pH conditions (e.g., pH 6 to 8), M in Z is typically a free anion (i.e., Z is —N+(R)2—V—SO3−). Under strongly acidic conditions (e.g, pH of up to 4), M in Z is hydrogen.

In any of the aforementioned embodiments containing a V group, each V is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl. In some of these embodiments, V is alkylene (e.g., having up to 6, 4, or 3 carbon atoms).

In any of the aforementioned embodiments containing a R group, each R is independently hydrogen, alkyl, or aryl, wherein alkyl may optionally be interrupted by —O— or substituted with hydroxyl or aryl, or two R groups taken together with the N atom to which they are attached can form a heterocyclic ring having 5 to 7 carbon atoms and optionally containing —O— or —S—. In some embodiments, each R is independently hydrogen or alkyl having up to 4 carbon atoms. In some embodiments, each R is independently alkyl having up to four carbon atoms (e.g., methyl or ethyl). Exemplary heterocyclic rings having 5 to 7 carbon atoms include pyrrolium, pyrimidinium, isoxazolium, oxazolium, thiazolium, isothiazolium, pyridinium, pyrrolidinium, piperidinium, morpholinium, and azepinium).

In any of the aforementioned embodiments containing a R1 group, each R1 is independently hydrogen or methyl.

In any of the aforementioned embodiments containing a Q1 group, each Q1 is independently —O—, —S—, or —N(R″)—, wherein R″ is hydrogen or alkyl having up to 6 carbon atoms. In some embodiments, Q1 is —O—.

Some fluorinated amphoteric compounds are commercially available. For example, a fluorinated betaine is available from E. I. du Pont de Nemours and Co., Wilmington, Del., under the trade designation “ZONYL FS-500” and a fluorinated amphoteric compound is available from 3M Company, St. Paul, Minn. under the trade designation “3M MIST CONTROL AGENT FC-1100”. Other fluorinated amphoteric compounds can be prepared, for example, by known methods. For example, fluorinated sulfonyl fluorides (e.g., perfluoro-1-butanesulfonyl fluoride, which is available from Sigma-Aldrich, St. Louis, Mo., and perfluoro-1-hexanesulfonyl fluoride) and fluorinated carboxylic acids or their derivatives can be treated with an amine having formula NH2—W—NR2 (e.g., 3-(dimethylamino)propylamine) in a first step to provide an amino-functionalized carboxamide or sulfonamide, which can then be treated with 1,3-propanesultone, acrylic acid, chloroacetic acid, or 2-bromoethanesulfonic acid using the methods described in U.S. Pat. No. 5,144,069 (Stern et al.) and U.S. Pat. No. 5,468,353 (Anich et al.), the disclosure of which methods are incorporated herein by reference. The preparation of perfluoropolyether betaines and sulfobetaines is reported in U.S. Pat. No. 3,839,425, the disclosure of which is incorporated herein by reference.

Some fluorinated carboxylic acids and fluorinated acid fluorides that may be useful for reaction with an amine having formula NH2—W—NR2 are commercially available (e.g., carboxylic acids of formula CF3—[O—CF2]1-3C(O)OH, available, for example, from Anles Ltd., St. Petersburg, Russia, and acid fluorides of formulas C2F5—O—(CF2)2—C(O)F, C3F7—O—(CF2)2—C(O)F and CF3CF2—O—CF2CF2—O—CF2C(O)F, available, for example, from Exfluor, Round Rock, Tex.). In some embodiments of the methods and the hydrocarbon-bearing formations disclosed herein, Rf is a perfluorinated polyether group of formula: CF3CF2CF2—O—[CF(CF3)CF2O]x—CF(CF3)—, wherein x is as defined above. Fluorinated acids of this type can be prepared by oligomerization of hexafluoropropylene oxide to provide a perfluoropolyether carbonyl fluoride.

Fluorinated carboxylic acids that are useful for preparing the fluorinated amphoteric compounds disclosed herein can also be prepared, for example, starting from fluorinated ether olefins represented by formula Rfe—(O)t—CF═CF2, wherein Rfe represents a partially or fully fluorinated alkyl group having from 1 to 10 carbon atoms and optionally interrupted with at least one oxygen atom, and t is 0 or 1, with the proviso that when t is 0, then Rfe is interrupted with at least one oxygen atom. Numerous fluorinated ether olefins are known (e.g., perfluorinated vinyl ethers and perfluorinated allyl ethers), and many can be obtained from commercial sources (e.g., 3M Company, St. Paul, Minn., and E.I. du Pont de Nemours and Company, Wilmington, Del.). Others can be prepared by known methods; (see, e.g., U.S. Pat. No. 5,350,497 (Hung et al.) and U.S. Pat. No. 6,255,536 (Worm et al.)).

Fluorinated ether olefins represented by formula Rfe—(O)t—CF═CF2 can be treated, for example, with a base (e.g., ammonia, alkali metal hydroxides, and alkaline earth metal hydroxides) to provide a fluorinated acid represented by formula Rfe—(O)t—CHF—C(O)OH. When the reaction is carried out in an aliphatic alcohol (e.g., methanol, ethanol, n-butanol, and t-butanol) in an alkaline medium, the resulting ether can be decomposed under acidic conditions to provide a fluorinated carboxylic acid of formula Rfe—(O)t—CHF—C(O)OH. Fluorinated acids represented by formula Rfe—(O)t—CHF—CF2—C(O)OH can be prepared, for example, by a free radical reaction of the fluorinated ether olefin represented by formula Rfe—(O)t—CF═CF2 with methanol followed by an oxidation of the resulting reaction product using conventional methods. Conditions for these reactions are described, for example, in U.S. Pat. App. No. 2007/0015864 (Hintzer et al.), the disclosure of which, relating to the preparation of compounds of formula Rfe—(O)t—CHF—CF2—C(O)OH, is incorporated herein by reference.

Fluorinated vinyl ethers represented by formula Rfe—O—CF═CF2 can be oxidized (e.g., with oxygen) in the presence of a fluoride source (e.g., antimony pentafluoride) to carboxylic acid fluorides of formula Rfe—O—CF2C(O)F according to the methods described in U.S. Pat. No. 4,987,254 (Schwertfeger et al.), in column 1, line 45 to column 2, line 42, the disclosure of which is incorporated herein by reference. Examples of compounds that can be prepared according to this method include CF3—(CF2)2—O—CF2—C(O)—CH3 and CF3—O—(CF2)3—O—CF2—C(O)—CH3, which are described in U.S. Pat. No. 2007/0015864 (Hintzer et al.), the disclosure of which, relating to the preparation of these compounds, is incorporated herein by reference. These esters can be converted to the corresponding carboxylic acids using, for example, conventional techniques.

Fluorinated carboxylic acids represented by formula CF3CFH—O—(CF2)p—C(O)OH, wherein p is 1 to 6, and their derivatives can be prepared, for example, by decarbonylation of difunctional perfluorinated acid fluoride according to the reaction:
FCOCF(CF3)—O—(CF2)pC(O)F→CF3—CHF—O—(CF2)pC(O)OH.
The reaction is typically carried out at an elevated temperature in the presence of water and base (e.g., a metal hydroxide or metal carbonate) according to known methods; see, e.g., U.S. Pat. No. 3,555,100 (Garth et al.), the disclosure of which, relating to the decarbonylation of difunctional acid fluorides, is incorporated herein by reference.

Compounds comprising first and second divalent units described above can also be prepared by conventional techniques. In some embodiments, the compound comprising first and second divalent units is a polymer having a weight average molecular weight in a range from 1,000 to 100,000, from 2,000 to 100,000, from 3,500 to 100,000, or from 10,000 to 75,000 grams per mole or in a range from 1,000 to 20,000, or from 2,000 to 10,000 grams per mole. Weight average molecular weights can be measured, for example, by gel permeation chromatography (i.e., size exclusion chromatography) using techniques known in the art. It will be appreciated by one skilled in the art that such polymers can exist as a mixture of compositions and molecular weights. In some embodiments, the first divalent units are present in a range from 25 to 99 (in some embodiments, from 35 to 99, from 50 to 99, from 60 to 98, from 75 to 97, or even from 85 to 97) based on the total weight of the compound (e.g., polymer). A first divalent unit is typically introduced into fluorinated amphoteric compound useful for practicing the present disclosure by reacting a monomer represented by formula CH2═C(R1)—C(O)—O-Q-Rf1, for example, under free-radical conditions. Fluorochemical monomers represented by this formula and methods for the preparation thereof are known in the art (see, e.g., U.S. Pat. No. 2,803,615 (Ahlbrecht et al.), the disclosure of which is incorporated herein by reference). Further examples of such compounds include acrylates or methacrylates derived from fluorochemical telomer alcohols, acrylates or methacrylates derived from fluorochemical carboxylic acids or esters, and perfluoroalkyl acrylates or methacrylates as disclosed in U.S. Pat. No. 5,852,148 (Behr et al.), the disclosure of which is incorporated herein by reference. Fluorochemical carboxylic acids or esters containing polyfluoropolyether groups can be converted into acrylates or methacrylates using the techniques described in US Patent Application No. 2007/0243389 (Audenaert et al.), sections (0083) to (0085) and (0092) to (0094), incorporated herein by reference.

Some useful monomers represented by formula CH2═C(R1)—C(O)—O-Q-Rf1 include C4F9SO2N(CH3)C2H4OC(O)CH═CH2, C4F9SO2N(CH3)C2H4OC(O)C(CH3)═CH2, C5F11SO2N(C2H5)C2H4OC(O)CH═CH2, C6F13SO2N(C2H5)C2H4OC(O)C(CH3)═CH2, C3F7SO2N(C4F19)C2H4OC(O)CH═CH2, C4F9CH2CH2OC(O)CH═CH2, C5F11CH2OC(O)CH═CH2, C6F13CH2CH2OC(O)CH═CH2, CF3(CF2)2CH2OC(O)CH═CH2, CF3(CF2)2CH2OC(O)C(CH3)═CH2, CF3(CF2)3CH2OC(O)C(CH3)═CH2, CF3(CF2)3CH2OC(O)CH═CH2, CF3(CF2)3S(O)2N(Ra)—(CH2)2—OC(O)CH═CH2, CF3(CF2)3S(O)2N(Ra)—(CH2)2—OC(O)C(CH3)═CH2, CF3CF2(CF2CF2)2-8(CH2)2OC(O)CH═CH2, and F(CF(CF3)CF2O)6.85CF(CF3)C(O)NHCH2CH2OC(O)CH═CH2, wherein Ra represents methyl, ethyl or n-butyl.

Second divalent units can be incorporated into fluorinated amphoteric compounds useful for practicing the present disclosure by copolymerization of a compound of formula CH2═C(R1)—C(O)—O-Q-Rf1 with a compound of formula N(R)2—V-Q1C(O)—C(R1)═CH2. Useful compounds of formula N(R)2—V-Q1C(O)—C(R1)═CH2 include aminoalkyl (meth)acrylates such as N,N-diethylaminoethylmethacrylate, N,N′-dimethylaminoethylmethacrylate and N-t-butylaminoethylmethacrylate, which are commercially available, for example, from Sigma-Aldrich and can be treated with 1,3-propanesultone or acrylic acid using the methods described above.

Compounds comprising first and second divalent units may, in some embodiments, comprise third divalent units represented by formula:


wherein each R2 is independently hydrogen or methyl, and wherein each R3 is independently alkyl having from 1 to 30 (in some embodiments, 1 to 25, 1 to 20, 1 to 10, 4 to 25, 8 to 25, or even 12 to 25) carbon atoms. Such third divalent units can be incorporated into a fluorinated amphoteric compound using a monomer selected from alkyl acrylates and methacrylates (e.g., octadecyl methacrylate, lauryl methacrylate, butyl acrylate, isobutyl methacrylate, ethylhexyl acrylate, ethylhexyl methacrylate, methyl methacrylate, hexyl acrylate, heptyl methacrylate, cyclohexyl methacrylate, or isobornyl acrylate) can be added to the reaction mixture comprising the monomer represented by formula CH2═C(R1)—C(O)—O-Q-Rf1.

Fluorinated amphoteric compounds comprising first and second divalent units useful for practicing the present disclosure may contain other units, typically in weight percents up to 20, 15, 10, or 5 percent, based on the total weight of the fluorinated amphoteric compound. These units may be incorporated into the compound by selecting additional components for the free-radical reaction such as allyl esters (e.g., allyl acetate and allyl heptanoate); vinyl ethers or allyl ethers (e.g., cetyl vinyl ether, dodecylvinyl ether, 2-chloroethylvinyl ether, or ethylvinyl ether); alpha-beta unsaturated nitriles (e.g., acrylonitrile, methacrylonitrile, 2-chloroacrylonitrile, 2-cyanoethyl acrylate, or alkyl cyanoacrylates); alpha-beta-unsaturated carboxylic acid derivatives (e.g., allyl alcohol, allyl glycolate, acrylamide, methacrylamide, n-diisopropyl acrylamide, or diacetoneacrylamide), styrene and its derivatives (e.g., vinyltoluene, alpha-methylstyrene, or alpha-cyanomethyl styrene); olefinic hydrocarbons which may contain at least one halogen (e.g., ethylene, propylene, isobutene, 3-chloro-1-isobutene, butadiene, isoprene, chloro and dichlorobutadiene, 2,5-dimethyl-1,5-hexadiene, and vinyl and vinylidene chloride); and hydroxyalkyl-substituted polymerizable compounds (e.g., 2-hydroxyethyl methacrylate).

Compounds comprising first and second divalent units useful for practicing the present disclosure can conveniently be prepared through a free radical reaction of a monomer represented by formula CH2═C(R1)—C(O)—O-Q-Rf1 with a compound of formula N(R)2—V-Q1C(O)—C(R1)═CH2 and optionally a non-fluorinated monomer (e.g., an alkyl acrylate or methacrylate) using methods known in the art. Free radical initiators such as those widely known and used in the art may be used to initiate reaction of the components. Examples of free-radical initiators include azo compounds (e.g., 2,2′-azobisisobutyronitrile (AIBN), 2,2′-azobis(2-methylbutyronitrile), or azo-2-cyanovaleric acid); hydroperoxides (e.g., cumene, tert-butyl or tert-amyl hydroperoxide); dialkyl peroxides (e.g., di-tert-butyl or dicumylperoxide); peroxyesters (e.g., tert-butyl perbenzoate or di-tert-butyl peroxyphthalate); diacylperoxides (e.g., benzoyl peroxide or lauryl peroxide). Useful photoinitiators include benzoin ethers (e.g., benzoin methyl ether or benzoin butyl ether); acetophenone derivatives (e.g., 2,2-dimethoxy-2-phenylacetophenone or 2,2-diethoxyacetophenone); and acylphosphine oxide derivatives and acylphosphonate derivatives (e.g., diphenyl-2,4,6-trimethylbenzoylphosphine oxide, isopropoxyphenyl-2,4,6-trimethylbenzoylphosphine oxide, or dimethyl pivaloylphosphonate). When heated or photolyzed such free-radical initiators fragment to generate free radicals which add to ethylenically unsaturated bonds and initiate free-radical reactions.

Free-radical reactions may be carried out in any suitable solvent at any suitable concentration, (e.g., from about 5 percent to about 90 percent by weight based on the total weight of the reaction mixture). Examples of suitable solvents include aliphatic and alicyclic hydrocarbons (e.g., hexane, heptane, cyclohexane), aromatic solvents (e.g., benzene, toluene, xylene), ethers (e.g., diethyl ether, glyme, diglyme, diisopropyl ether), esters (e.g., ethyl acetate, butyl acetate), alcohols (e.g., ethanol, isopropyl alcohol), ketones (e.g., acetone, methyl ethyl ketone, methyl isobutyl ketone), sulfoxides (e.g., dimethyl sulfoxide), amides (e.g., N,N-dimethylformamide, N,N-dimethylacetamide), halogenated solvents (e.g., methylchloroform, 1,1,2-trichloro-1,2,2-trifluoroethane, trichloroethylene or trifluorotoluene), and mixtures thereof.

While it is not practical to enumerate a particular temperature suitable for all initiators and all solvents, generally suitable temperatures are in a range from about 30° C. to about 200° C. Particular temperature and solvents for use can be selected by those skilled in the art based on considerations such as the solubility of reagents, the temperature required for the use of a particular initiator, and the molecular weight desired.

Typical chain transfer agents that may be used in the preparation of polymeric fluorinated amphorteric compounds herein include hydroxyl-substituted mercaptans (e.g., 2-mercaptoethanol, 3-mercapto-2-butanol, 3-mercapto-2-propanol, 3-mercapto-1-propanol, and 3-mercapto-1,2-propanediol (i.e., thioglycerol)); difunctional mercaptans (e.g., di(2-mercaptoethyl)sulfide); and aliphatic mercaptans (e.g., octylmercaptan, dodecylmercaptan, and octadecylmercaptan).

Adjusting, for example, the concentration and activity of the initiator, the concentration of each of the reactive monomers, the temperature, the concentration of the chain transfer agent, and the solvent using techniques known in the art can control the molecular weight of a polyacrylate copolymer.

Typically, in treatment compositions useful for practicing the methods described herein, the fluorinated amphoteric compound is present in the treatment composition at at least 0.01, 0.015, 0.02, 0.025, 0.03, 0.035, 0.04, 0.045, 0.05, 0.055, 0.06, 0.065, 0.07, 0.075, 0.08, 0.085, 0.09, 0.095, 0.1, 0.15, 0.2, 0.25, 0.5, 1, 1.5, 2, 3, 4, or 5 percent by weight, up to 5, 6, 7, 8, 9, or 10 percent by weight, based on the total weight of the treatment composition. For example, the amount of the fluorinated amphoteric compound in the treatment compositions may be in a range of from 0.01 to 10, 0.1 to 10, 0.1 to 5, 1 to 10, or even in a range from 1 to 5 percent by weight, based on the total weight of the treatment composition. The methods disclosed herein have been found to be surprisingly effective even with low concentrations of the fluorinated amphoteric compound. For example, the amount of the fluorinated amphoteric compound in the treatment composition may be in a range of from 0.01 to 0.95, 0.1 to 0.95, 0.3 to 0.9, 0.3 to 0.85, or even in a range from 0.4 to 0.8 percent by weight, based on the total weight of the treatment composition.

Treatment compositions useful in practicing the methods disclosed herein comprise solvent. Examples of useful solvents include organic solvents, water, easily gasified fluids (e.g., supercritical or liquid carbon dioxide, ammonia, or low-molecular-weight hydrocarbons), and combinations thereof. In some embodiments, the treatment compositions comprise water and at least one organic solvent. In some embodiments, the treatment compositions are essentially free of water (i.e., contains less than 0.1 percent by weight of water, based on the total weight of the composition). In some embodiments, the solvent is a water-miscible solvent (i.e., the solvent is soluble in water in all proportions). Examples of organic solvents include polar and/or water-miscible solvents, for example, monohydroxy alcohols having from 1 to 4 or more carbon atoms (e.g., methanol, ethanol, isopropanol, propanol, or butanol); polyols such as glycols (e.g., ethylene glycol or propylene glycol), terminal alkanediols (e.g., 1,3-propanediol, 1,4-butanediol, 1,6-hexanediol, or 1,8-octanediol), polyglycols (e.g., diethylene glycol, triethylene glycol, dipropylene glycol, or polypropylene glycol)), triols (e.g., glycerol, trimethylolpropane), or pentaerythritol; ethers such as diethyl ether, methyl t-butyl ether, tetrahydrofuran, p-dioxane, or polyol ethers (e.g., glycol ethers (e.g., ethylene glycol monobutyl ether, diethylene glycol monomethyl ether, dipropylene glycol monomethyl ether, propylene glycol monomethyl ether, 2-butoxyethanol, or those glycol ethers available under the trade designation “DOWANOL” from Dow Chemical Co., Midland, Mich.)); ketones (e.g., acetone or 2-butanone); and combinations thereof.

In some embodiments, the solvent comprises at least one of a polyol or polyol ether independently having from 2 to 25 (in some embodiments, 2 to 15, 2 to 10, 2 to 9, or even 2 to 8) carbon atoms. In some embodiments, the solvent comprises a polyol. The term “polyol” refers to an organic molecule consisting of C, H, and O atoms connected one to another by C—H, C—C, C—O, O—H single bonds, and having at least two C—O—H groups. In some embodiments, useful polyols have 2 to 25, 2 to 20, 2 to 15, 2 to 10, 2 to 8, or even 2 to 6 carbon atoms. In some embodiments, the solvent comprises a polyol ether. The term “polyol ether” refers to an organic molecule consisting of C, H, and O atoms connected one to another by C—H, C—C, C—O, O—H single bonds, and which is at least theoretically derivable by at least partial etherification of a polyol. In some embodiments, the polyol ether has at least one C—O—H group and at least one C—O—C linkage. Useful polyol ethers may have from 3 to 25 carbon atoms, 3 to 20, 3 to 15, 3 to 10, 3 to 9, 3 to 8, or even from 5 to 8 carbon atoms. In some embodiments, the polyol is at least one of ethylene glycol, propylene glycol, polypropylene glycol), 1,3-propanediol, or 1,8-octanediol, and the polyol ether is at least one of 2-butoxyethanol, diethylene glycol monomethyl ether, ethylene glycol monobutyl ether, dipropylene glycol monomethyl ether, or 1-methoxy-2-propanol. In some embodiments, the polyol and/or polyol ether has a normal boiling point of less than 450° F. (232° C.), which may be useful, for example, to facilitate removal of the polyol and/or polyol ether from a well after treatment.

In some embodiments, useful solvents for practicing the methods disclosed herein comprise at least one of water, a monohydroxy alcohol, an ether, or a ketone, wherein the monohydroxy alcohol, the ether, and the ketone each independently have up to 4 carbon atoms. Exemplary monohydroxy alcohols having from 1 to 4 carbon atoms include methanol, ethanol, n-propanol, isopropanol, 1-butanol, 2-butanol, isobutanol, and t-butanol. Exemplary ethers having from 2 to 4 carbon atoms include diethyl ether, ethylene glycol methyl ether, tetrahydrofuran, p-dioxane, and ethylene glycol dimethyl ether. Exemplary ketones having from 3 to 4 carbon atoms include acetone, 1-methoxy-2-propanone, and 2-butanone. In some embodiments, useful solvents for practicing the methods disclosed herein comprise at least one of methanol, ethanol, isopropanol, tetrahydrofuran, or acetone.

In some embodiments of the methods disclosed herein, the treatment compositions comprise at least two organic solvents. In some embodiments, the treatment compositions comprise at least one of a polyol or polyol ether independently having from 2 to 25 (in some embodiments, 2 to 15, 2 to 10, 2 to 9, or even 2 to 8) carbon atoms and at least one of water, a monohydroxy alcohol, an ether, or a ketone, wherein the monohydroxy alcohol, the ether, and the ketone each independently have up to 4 carbon atoms. In these embodiments, in the event that a component of the solvent is a member of two functional classes, it may be used as either class but not both. For example, ethylene glycol methyl ether may be a polyol ether or a monohydroxy alcohol, but not both simultaneously. In these embodiments, each solvent component may be present as a single component or a mixture of components. In some embodiments, compositions useful for practicing the methods disclosed herein comprise at least one of a polyol or polyol ether independently having from 2 to 25 (in some embodiments, 2 to 15, 2 to 10, 2 to 9, or even 2 to 8) carbon atoms and at least one monohydroxy alcohol having up to 4 carbon atoms. In some embodiments, the solvent consists essentially of (i.e., does not contain any components that materially affect water solubilizing or displacement properties of the composition under downhole conditions) at least one of a polyol having from 2 to 25 (in some embodiments, 2 to 20, 2 to 15, 2 to 10, 2 to 9, 2 to 8, or even 2 to 6) carbon atoms or polyol ether having from 3 to 25 (in some embodiments, 3 to 20, 3 to 15, 3 to 10, 3 to 9, 3 to 8, or even from 5 to 8) carbon atoms, and at least one monohydroxy alcohol having from 1 to 4 carbon atoms, ether having from 2 to 4 carbon atoms, or ketone having from 3 to 4 carbon atoms. Typically, the solvents described herein are capable of solubilizing more brine in the presence of fluorinated amphoteric compound than methanol alone.

In some embodiments of methods according to the present disclosure, useful solvents at least one of at least partially solubilize or at least partially displace brine in the hydrocarbon-bearing formation. By the term “solubilizes”, it is meant that the solvent dissolves the water and the salts in the brine. “At least partially solubilize” includes dissolving all or nearly all (e.g., at least 95% including up to 100%) of the water and the salts in the brine. In some embodiments, useful solvents at least partially solubilize or at least partially displace liquid hydrocarbons in the hydrocarbon-bearing formation.

For any of the embodiments wherein the treatment compositions useful for practicing the methods disclosed herein comprise at least one of a polyol or polyol ether independently having from 2 to 25 (in some embodiments, 2 to 15, 2 to 10, 2 to 9, or even 2 to 8) carbon atoms, the polyol or polyol ether is present in the treatment composition at at least 50, 55, 60, or 65 percent by weight and up to 75, 80, 85, or 90 percent by weight, based on the total weight of the composition. In some embodiments, the treatment composition comprises up to 50, 40, 30, 20, or even 10 percent by weight of a monohydroxy alcohol having up to 4 carbon atoms, based on the total weight of the treatment composition.

Useful combinations of two solvents include 1,3-propanediol (80%)/isopropanol (IPA) (20%), propylene glycol (70%)/IPA (30%), propylene glycol (90%)/IPA (10%), propylene glycol (80%)/IPA (20%), ethylene glycol (50%)/ethanol (50%), ethylene glycol (70%)/ethanol (30%), propylene glycol monobutyl ether (PGBE) (50%)/ethanol (50%), PGBE (70%)/ethanol (30%), dipropylene glycol monomethyl ether (DPGME) (50%)/ethanol (50%), DPGME (70%)/ethanol (30%), diethylene glycol monomethyl ether (DEGME) (70%)/ethanol (30%), triethylene glycol monomethyl ether (TEGME) (50%)/ethanol (50%), TEGME (70%)/ethanol (30%), 1,8-octanediol (50%)/ethanol (50%), propylene glycol (70%)/tetrahydrofuran (THF) (30%), propylene glycol (70%)/acetone (30%), propylene glycol (70%), methanol (30%), propylene glycol (60%)/IPA (40%), 2-butoxyethanol (80%)/ethanol (20%), 2-butoxyethanol (70%)/ethanol (30%), 2-butoxyethanol (60%)/ethanol (40%), propylene glycol (70%)/ethanol (30%), ethylene glycol (70%)/IPA (30%), and glycerol (70%)/IPA (30%), wherein the exemplary percentages are by weight are based on the total weight of solvent.

In some embodiments of treatment compositions disclosed herein, the solvent comprises a ketone, ether, or ester having from 4 to 10 (e.g., 5 to 10, 6 to 10, 6 to 8, or 6) carbon atoms or a hydrofluoroether or hydrofluorocarbon. In some of these embodiments, the solvent comprises two different ketones, each having 4 to 10 carbon atoms (e.g., any combination of 2-butanone, 4-methyl-2-pentanone, 3-methyl-2-pentanone, 2-methyl-3-pentanone, and 3,3-dimethyl-2-butanone). In some embodiments, the solvent further comprises at least one of water or a monohydroxy alcohol having up to 4 carbon atoms (e.g., methanol, ethanol, n-propanol, isopropanol, 1-butanol, 2-butanol, isobutanol, and t-butanol). Useful ethers having 4 to 10 carbon atoms include diethyl ether, diisopropyl ether, tetrahydrofuran, p-dioxane, and tert-butyl methyl ether. Useful esters having 4 to 10 carbon atoms include ethyl acetate, propyl acetate, and butyl acetate. Useful hydrofluoroethers may be represented by the general formula Rf3—[O—Rh]a, wherein a is an integer from 1 to 3; Rf3 is a perfluoroalkyl or di- or trivalent perfluoroalkylene, each of which may be interrupted with at least one —O—; and Rh is an alkyl group optionally interrupted with at least one —O—. Numerous hydrofluoroethers of this type are disclosed in U.S. Pat. No. 6,380,149 (Flynn et al.), the disclosure of which is incorporated herein by reference. In some embodiments, the hydrofluoroether is methyl perfluorobutyl ether or ethyl perfluorobutyl ether. Useful hydrofluoroethers also include hydrofluoroethers available, for example, from 3M Company, St. Paul, Minn., under the trade designations “HFE-7100” and “HFE-7200”.

The ingredients for treatment compositions described herein including fluorinated amphoteric compounds and solvents can be combined using techniques known in the art for combining these types of materials, including using conventional magnetic stir bars or mechanical mixer (e.g., in-line static mixer and recirculating pump).

The amount of solvent typically varies inversely with the amount of other components in treatment compositions useful in practicing any of the methods disclosed herein. For example, based on the total weight of the treatment composition the solvent may be present in the treatment composition in an amount of from at least 10, 20, 30, 40, or 50 percent by weight or more up to 60, 70, 80, 90, 95, 98, or even 99 percent by weight, or more.

Generally, the amounts of the fluorinated amphoteric compound and solvent (and type of solvent) is dependent on the particular application since conditions typically vary between wells, at different depths of individual wells, and even over time at a given location in an individual well. Advantageously, treatment methods according to the present disclosure can be customized for individual wells and conditions.

In some embodiments of the methods disclosed herein, the hydrocarbon-bearing formation includes brine. The brine present in the formation may be from a variety of sources including at least one of connate water, flowing water, mobile water, immobile water, residual water from a fracturing operation or from other downhole fluids, or crossflow water (e.g., water from adjacent perforated formations or adjacent layers in the formation). In some embodiments, the brine is connate water. In some embodiments, the brine causes water blocking (i.e., declining productivity resulting from increasing water saturation in a well). It is believed that useful treatment compositions will not undergo precipitation of the fluorinated amphoteric compounds, dissolved salts, or other solids when the treatment compositions encounter the brine. Such precipitation may inhibit the adsorption or reaction of the fluorinated amphoteric compound on the formation, may clog the pores in the hydrocarbon-bearing formation thereby decreasing the permeability and the hydrocarbon and/or brine production, or a combination thereof.

In some embodiments, methods according to the present disclosure include receiving (e.g., obtaining or measuring) data comprising the temperature and the brine composition (including the brine saturation level and components of the brine) of a selected hydrocarbon-bearing formation. These data can be obtained or measured using techniques well known to one skilled in the art. In some embodiments, the methods comprise selecting a treatment composition for the hydrocarbon-bearing formation comprising the fluorinated amphoteric compound and solvent, based on the behavior of a mixture of the brine composition and the treatment composition. Typically, for the methods disclosed herein, a mixture of an amount of brine and the treatment composition is transparent and substantially free of precipitated solid (e.g., salts, asphaltenes, or fluorinated amphoteric compounds). Although not wanting to be bound by theory, it is believed that the effectiveness of the methods disclosed herein for improving hydrocarbon productivity of a particular oil and/or gas well having brine accumulated in the near wellbore region will typically be determined by the ability of the treatment composition to dissolve the quantity of brine present in the near wellbore region of the well. Hence, at a given temperature greater amounts of treatment compositions having lower brine solubility (i.e., treatment compositions that can dissolve a relatively lower amount of brine) will typically be needed than in the case of treatment compositions having higher brine solubility and containing the same fluorinated amphoteric compound at the same concentration.

In some embodiments, a mixture of an amount of the brine composition and the treatment composition, at the temperature of the hydrocarbon-bearing formation, is transparent and free of precipitated solids. As used herein, the term transparent refers to allowing clear view of objects beyond. In some embodiments, transparent refers to liquids that are not hazy or cloudy. The term “substantially free of precipitated solid” refers to an amount of precipitated solid that does not interfere with the ability of the fluorinated amphoteric compound to increase the gas or liquid permeability of the hydrocarbon-bearing formation. In some embodiments, “substantially free of precipitated solid” means that no precipitated solid is visually observed. In some embodiments, “substantially free of precipitated solid” is an amount of solid that is less than 5% by weight higher than the solubility product at a given temperature and pressure.

In some embodiments, the transparent mixture of the brine composition and the treatment composition does not separate into layers, and in other embodiments, the transparent mixture of the brine composition and the treatment composition separates into at least two separate transparent liquid layers. Phase behavior of a mixture of the brine composition and the treatment composition can be evaluated prior to treating the hydrocarbon-bearing formation by obtaining a sample of the brine from the hydrocarbon-bearing formation and/or analyzing the composition of the brine from the hydrocarbon-bearing formation and preparing an equivalent brine having the same or similar composition to the composition of the brine in the formation. The brine composition and the treatment composition can be combined (e.g., in a container) at the temperature and then mixed together (e.g., by shaking or stirring). The mixture is then maintained at the temperature for a certain time period (e.g., 15 minutes), removed from the heat, and immediately visually evaluated to see if phase separation, cloudiness, or precipitation occurs. The amount of the brine composition in the mixture may be in a range from 5 to 95 percent by weight (e.g., at least 10, 20, 30, percent by weight and up to 35, 40, 45, 50, 55, 60, or 70 percent by weight) based on the total weight of the mixture.

Whether the mixture of the brine composition and the treatment composition is transparent, substantially free of precipitated solid, and separates into layers at the temperature of the hydrocarbon-bearing formation can depend on many variables (e.g., concentration of the fluorinated amphoteric compound, solvent composition, brine concentration and composition, hydrocarbon concentration and composition, and the presence of other components (e.g., surfactants or scale inhibitors)). Typically, for treatment compositions comprising at least one of a polyol or polyol ether described above and a monohydroxy alcohol having up to 4 carbon atoms, mixtures of the brine composition and the treatment composition do not separate into two or more layers. In some of these embodiments, the salinity of the brine is less than 150,000 ppm (e.g., less than 140,000, 130,000, 120,000, or 110,000 ppm) total dissolved salts. Typically, for treatment compositions described above comprising at least one (e.g., one or two) ketone having from 4 to 10 carbon atoms or a hydrofluoroether, mixtures of the brine composition and the treatment composition separate into two or more layers. In some of these embodiments, the salinity of the brine is greater than 100,000 ppm (e.g., greater than 110,000, 125,000, 130,000, or 150,000 ppm) total dissolved salt. Although not wishing to be bound by theory, it is believed that when two or more layers form in such mixtures, the fluorinated amphoteric compound preferentially partitions into a layer rich in organic solvent that has a lower concentration of dissolved salts. Typically, treatment compositions comprising at least one of a polyol or polyol ether described above and treatment compositions comprising at least one ketone having from 4 to 10 carbon atoms or a hydrofluoroether are capable of solubilizing more brine (i.e., no salt precipitation occurs) in the presence of a fluorinated amphoteric compound than methanol, ethanol, propanol, butanol, or acetone alone.

The phase behavior of the composition and the brine can be evaluated over an extended period of time (e.g., 1 hour, 12 hours, 24 hours, or longer) to determine if any phase separation, precipitation, or cloudiness is observed. By adjusting the relative amounts of brine (e.g., equivalent brine) and the treatment composition, it is possible to determine the maximum brine uptake capacity (above which precipitation occurs) of the treatment composition at a given temperature. Varying the temperature at which the above procedure is carried out typically results in a more complete understanding of the suitability of treatment compositions for a given well.

In addition to using a phase behavior evaluation, it is also contemplated that one may be able to obtain the compatibility information, in whole or in part, by computer simulation or by referring to previously determined, collected, and/or tabulated information (e.g., in a handbook, table, or a computer database). In some embodiments, the selecting a treatment composition comprises consulting a table of compatibility data between brines and treatment compositions at different temperatures.

In some embodiments of the methods disclosed herein, the fluorinated amphoteric compound is present in an amount sufficient to increase at least the gas permeability of the hydrocarbon-bearing formation. Before contacting the hydrocarbon-bearing formation with the treatment composition, the hydrocarbon-bearing formation typically has at least one of brine or liquid hydrocarbons. In some embodiments, the gas permeability after contacting the hydrocarbon-bearing formation with the treatment composition is increased by at least 5 percent (in some embodiments, by at least 10, 15, 20, 30, 40, 50, 60, 70, 80, 90, or even 100 percent or more) relative to the gas permeability of the formation before contacting the formation with the treatment composition. In some embodiments, the gas permeability is a gas relative permeability. In some embodiments, the liquid (e.g., oil or condensate) permeability in the hydrocarbon-bearing formation is also increased (in some embodiments, by at least 5, 10, 15, 20, 30, 40, 50, 60, 70, 80, 90, or even 100 percent or more) after contacting the formation with the treatment composition.

Since it has been reported that carbonate hydrocarbon-bearing formations are positively charged and have been reported to be treated with certain anionic compounds, it is unexpected that amphoteric compounds, which typically contain positively charged groups under neutral conditions, could be used to successfully treat carbonate hydrocarbon-bearing formations. Adsorption of amphoteric compounds disclosed herein onto carbonates is evidenced by the Examples, below, where it is shown that even after several volumes of hexane are passed through a column of calcium carbonate, an increase in permeability after treatment is maintained.

In some embodiments of the methods disclosed herein, hydrocarbon-bearing formations have both gas and liquid hydrocarbons. The liquid hydrocarbons in the hydrocarbon-bearing formation may be, for example, at least one of retrograde gas condensate or oil and may comprise, for example, at least one of methane, ethane, propane, butane, pentane, hexane, heptane, octane, nonane, decane, or higher hydrocarbons. In some of these embodiments, the liquid hydrocarbons may be condensate, black oil, or volatile oil. The term “black oil” refers to the class of crude oil typically having gas-oil ratios (GOR) less than about 2000 scf/stb (356 m3/m3). For example, a black oil may have a GOR in a range from about 100 (18), 200 (36), 300 (53), 400 (71), or even 500 scf/stb (89 m3/m3) up to about 1800 (320), 1900 (338), or even 2000 scf/stb (356 m3/m3). The term “volatile oil” refers to the class of crude oil typically having a GOR in a range between about 2000 and 3300 scf/stb (356 and 588 m3/m3). For example, a volatile oil may have a GOR in a range from about 2000 (356), 2100 (374), or even 2200 scf/stb (392 m3/m3) up to about 3100 (552), 3200 (570), or even 3300 scf/stb (588 m3/m3).

Methods according to the present disclosure may be practiced, for example, in a laboratory environment (e.g., on a core sample (i.e., a portion) of a hydrocarbon-bearing formation) or in the field (e.g., on a subterranean hydrocarbon-bearing formation situated downhole). Typically, the methods disclosed herein are applicable to downhole conditions having a pressure in a range from about 1 bar (100 kPa) to about 1000 bars (100 MPa) and have a temperature in a range from about 100° F. (37.8° C.) to 400° F. (204° C.) although the methods are not limited to hydrocarbon-bearing formations having these conditions. The skilled artisan, after reviewing the instant disclosure, will recognize that various factors may be taken into account in practice of the any of the disclosed methods including, for example, the ionic strength of the brine, pH (e.g., a range from a pH of about 4 to about 10), and the radial stress at the wellbore (e.g., about 1 bar (100 kPa) to about 1000 bars (100 MPa)).

In the field, contacting a hydrocarbon-bearing formation with a composition described herein can be carried out using methods (e.g., by pumping under pressure) well known to those skilled in the oil and gas art. Coil tubing, for example, may be used to deliver the treatment composition to a particular geological zone of a hydrocarbon-bearing formation. In some embodiments of practicing the methods described herein it may be desirable to isolate a geological zone (e.g., with conventional packers) to be contacted with the treatment composition.

Methods described herein are useful, for example on both existing and new wells. Typically, it is believed to be desirable to allow for a shut-in time after treatment compositions described herein are contacted with the hydrocarbon-bearing formations. Exemplary shut-in times include a few hours (e.g., 1 to 12 hours), about 24 hours, or even a few (e.g., 2 to 10) days. After the treatment composition has been allowed to remain in place for a selected time, the solvents present in the composition may be recovered from the formation by simply pumping fluids up tubing in a well as is commonly done to produce fluids from a formation.

In some embodiments of methods according to the present disclosure, the method comprises contacting the hydrocarbon-bearing formation with a fluid prior to contacting the hydrocarbon-bearing formation with the treatment composition, wherein the fluid at least one of partially solubilizes or partially displaces the brine in the hydrocarbon-bearing formation. In some embodiments, the fluid partially solubilizes the brine. In some embodiments, the fluid partially displaces the brine. In some embodiments, the fluid is substantially free of fluorinated surfactants. The term “substantially free of fluorinated surfactants” refers to fluid that may have a fluorinated surfactant in an amount insufficient for the fluid to have a cloud point (e.g., when it is below its critical micelle concentration). A fluid that is substantially free of fluorinated surfactants may be a fluid that has a fluorinated surfactant but in an amount insufficient to alter the wettability of, for example, a hydrocarbon-bearing formation under downhole conditions. A fluid that is substantially free of fluorinated surfactants includes those that have a weight percent of such surfactants as low as 0 weight percent. The fluid may be useful for decreasing the concentration of at least one of the salts present in a brine before introducing the treatment composition to the hydrocarbon-bearing formation. The change in brine composition may change the results of a phase behavior evaluation (e.g., the combination of a treatment composition with a first brine before the fluid preflush may result in salt precipitation while the combination of the treatment composition with the brine after the fluid preflush may result in a transparent mixture with no salt precipitation.) In some embodiments, the fluid comprises at least one of toluene, diesel, heptane, octane, or condensate. In some embodiments, the fluid comprises at least one of water, methanol, ethanol, or isopropanol. In some embodiments, the fluid comprises at least one of a polyol or polyol ether independently having from 2 to 25 carbon atoms. In some embodiments, useful polyols have 2 to 20, 2 to 15, 2 to 10, 2 to 8, or even 2 to 6 carbon atoms. Exemplary useful polyols include ethylene glycol, propylene glycol, polypropylene glycol), 1,3-propanediol, trimethylolpropane, glycerol, pentaerythritol, and 1,8-octanediol. In some embodiments, useful polyol ethers may have from 3 to 25 carbon atoms, 3 to 20, 3 to 15, 3 to 10, 3 to 8, or even from 5 to 8 carbon atoms. Exemplary useful polyol ethers include diethylene glycol monomethyl ether, ethylene glycol monobutyl ether, dipropylene glycol monomethyl ether, 2-butoxyethanol, and 1-methoxy-2-propanol. In some embodiments, the fluid comprises at least one monohydroxy alcohol, ether, or ketone independently having up to four carbon atoms. In some embodiments, the fluid comprises at least one of nitrogen, carbon dioxide, or methane.

In some embodiments, the fluid at least one of partially solubilizes or displaces the liquid hydrocarbons in the hydrocarbon-bearing formation.

In some embodiments of the methods disclosed herein, the hydrocarbon-bearing formation has at least one fracture. In some embodiments, fractured formations have at least 2, 3, 4, 5, 6, 7, 8, 9, or even 10 or more fractures. As used herein, the term “fracture” refers to a fracture that is manmade. In the field, for example, fractures are typically made by injecting a fracturing fluid into a subterranean geological formation at a rate and pressure sufficient to open a fracture therein (i.e., exceeding the rock strength). Typically, fracturing refers to hydraulic fracturing, and the fracturing fluid is a hydraulic fluid. Fracturing fluids may or may not contain proppants. Unintentional fracturing can sometimes occur, for example, during drilling of a wellbore. Unintentional fractures can be detected (e.g., by fluid loss from the wellbore) and repaired. Typically, fracturing a hydrocarbon-bearing formation refers to intentionally fracturing the formation after the wellbore is drilled. In some embodiments, hydrocarbon-bearing formations that may be treated according to the methods disclosed herein (e.g., limestone or carbonate formations) have natural fractures. Natural fractures may be formed, for example, as part of a network of fractures.

Fracturing of carbonate formations can also be carried out in the presence of acids (e.g., hydrochloric acid, acetic acid, formic acid or combinations thereof) to etch the open faces of induced fractures. When the treatment is complete and the fracture closes, the etched surface provides a high-conductivity path from the hydrocarbon-bearing formation or reservoir to the wellbore. Treatments are most commonly conducted with 15% or 28% solutions of hydrochloric acid. Applications for various acid types or blends are typically based on the reaction characteristics of the prepared treatment fluid. Fluorinated amphoteric compounds described herein may be useful in conjunction with acid treatments (e.g., before, during, or after the acid treatment) to modify the wettability of the fractured formation.

In some embodiments of the treatment methods disclosed herein, wherein contacting the formation with the treatment composition provides an increase in at least one of the gas permeability or the liquid permeability of the formation, the formation is a non-fractured formation (e.g., free of manmade fractures made by the hydraulic fracturing processes described herein). Advantageously, treatment methods disclosed herein typically provide an increase in at least one of the gas permeability or the liquid permeability of the formation without fracturing the formation.

In some of embodiments of the treatment methods disclosed herein, wherein the hydrocarbon-bearing formation has at least one fracture, the fracture has a plurality of proppants therein. Exemplary proppants known in the art include those made of sand (e.g., Ottawa, Brady or Colorado Sands, often referred to as white and brown sands having various ratios), resin-coated sand, sintered bauxite, ceramics (i.e., glasses, crystalline ceramics, glass-ceramics, and combinations thereof), thermoplastics, organic materials (e.g., ground or crushed nut shells, seed shells, fruit pits, and processed wood), and clay. Sand proppants are available, for example, from Badger Mining Corp., Berlin, Wis.; Borden Chemical, Columbus, Ohio; and Fairmont Minerals, Chardon, Ohio. Thermoplastic proppants are available, for example, from the Dow Chemical Company, Midland, Mich.; and BJ Services, Houston, Tex. Clay-based proppants are available, for example, from CarboCeramics, Irving, Tex.; and Saint-Gobain, Courbevoie, France. Sintered bauxite ceramic proppants are available, for example, from Borovichi Refractories, Borovichi, Russia; 3M Company, St. Paul, Minn.; CarboCeramics; and Saint Gobain. Glass bubble and bead proppants are available, for example, from Diversified Industries, Sidney, British Columbia, Canada; and 3M Company.

In some embodiments, the proppants form packs within a formation and/or wellbore. Proppants may be selected to be chemically compatible with the solvents and fluorinated amphoteric compounds described herein. The term “proppant” as used herein includes fracture proppant materials introducible into the formation as part of a hydraulic fracture treatment and sand control particulate introducible into the wellbore/formation as part of a sand control treatment such as a gravel pack or frac pack.

In some embodiments, methods according to the present disclosure include contacting the hydrocarbon-bearing formation with the treatment composition during fracturing, after fracturing, or during and after fracturing the hydrocarbon-bearing formation. In some of these embodiments, the fracturing fluid, which may contain proppants, may be aqueous (e.g., a brine) or may contain predominantly organic solvent (e.g., an alcohol or a hydrocarbon). In some embodiments, it may be desirable for the fracturing fluid to include viscosity enhancing agents (e.g., polymeric viscosifiers), electrolytes, corrosion inhibitors, scale inhibitors, and other such additives that are common to a fracturing fluid.

In some embodiments of methods of treated fractured formations, the amount of the composition introduced into the fractured formation is based at least partially on the volume of the fracture(s). The volume of a fracture can be measured using methods that are known in the art (e.g., by pressure transient testing of a fractured well). Typically, when a fracture is created in a hydrocarbon-bearing subterranean formation, the volume of the fracture can be estimated using at least one of the known volume of fracturing fluid or the known amount of proppant used during the fracturing operation. Coil tubing, for example, may be used to deliver the treatment composition to a particular fracture. In some embodiments, in practicing the methods disclosed herein it may be desirable to isolate the fracture (e.g., with conventional packers) to be contacted with the treatment composition.

In some embodiments, wherein the formation treated according to the methods described herein has at least one fracture, the fracture has a conductivity, and after the composition contacts at least one of the fracture or at least a portion of the plurality of proppants, the conductivity of the fracture is increased (e.g., by 25, 50, 75, 100, 125, 150, 175, 200, 225, 250, 275, or even by 300 percent).

Referring to FIG. 1, an exemplary offshore oil platform is schematically illustrated and generally designated 10. Semi-submersible platform 12 is centered over submerged hydrocarbon-bearing formation 14 located below sea floor 16. Subsea conduit 18 extends from deck 20 of platform 12 to wellhead installation 22 including blowout preventers 24. Platform 12 is shown with hoisting apparatus 26 and derrick 28 for raising and lowering pipe strings such as work string 30.

Wellbore 32 extends through the various earth strata including hydrocarbon-bearing formation 14. Casing 34 is cemented within wellbore 32 by cement 36. Work string 30 may include various tools including, for example, sand control screen assembly 38 which is positioned within wellbore 32 adjacent to hydrocarbon-bearing formation 14. Also extending from platform 12 through wellbore 32 is fluid delivery tube 40 having fluid or gas discharge section 42 positioned adjacent to hydrocarbon-bearing formation 14, shown with production zone 48 between packers 44, 46. When it is desired to treat the near-wellbore region of hydrocarbon-bearing formation 14 adjacent to production zone 48, work string 30 and fluid delivery tube 40 are lowered through casing 34 until sand control screen assembly 38 and fluid discharge section 42 are positioned adjacent to the near-wellbore region of hydrocarbon-bearing formation 14 including perforations 50. Thereafter, a composition described herein is pumped down delivery tube 40 to progressively treat the near-wellbore region of hydrocarbon-bearing formation 14.

While the drawing depicts an offshore operation, the skilled artisan will recognize that the methods for treating a production zone of a wellbore are equally well-suited for use in onshore operations. Also, while the drawing depicts a vertical well, the skilled artisan will also recognize that methods according to the present disclosure are equally well-suited for use in deviated wells, inclined wells or horizontal wells.

Selected Embodiments of the Disclosure

In a first embodiment, the present disclosure provides a method of treating a hydrocarbon-bearing formation, the method comprising:

contacting the hydrocarbon-bearing formation with a treatment composition comprising solvent and a fluorinated amphoteric compound, wherein the hydrocarbon-bearing formation comprises carbonate, and wherein the fluorinated amphoteric compound is selected from the group consisting of:

    • (a)

    • (b) Rf-Q-Z
    • (c) a compound comprising:
      • a first divalent unit represented by

      • and
      • a second divalent unit represented by formula


and

    • (d) combinations thereof;
      wherein

Rf is independently fluoroalkyl having up to 10 carbon atoms or a polyfluoropolyether group;

each Rf1 is independently fluoroalkyl having up to 10 carbon atoms or a polyfluoropolyether group;

X is —SO2— or —C(O)—;

Y is —N(R)2, —N+(R)3, or —N+(R)3A-, wherein A- is a counter anion;

Y′ is —P(O)(OM)2, —O—P(O)(OM)2, —SO3M, —O—SO3M, or —CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation;

    • each Q is independently —SO2—N(R′)—W—, —C(O)—N(R′)—W—, alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O—, —S—, —SO2— or —C(O)—;

each W is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl;

Z is —N+(R)2—V—SO3M, or —N+(R)2—V—CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation;

each V is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl;

each R is independently hydrogen, alkyl, or aryl, wherein alkyl may optionally be interrupted by —O— or substituted with hydroxyl or aryl, or two R groups taken together with the N atom to which they are attached can form a heterocyclic ring having up to six carbon atoms and optionally containing —O— or —S—;

R′ is hydrogen, alkyl having up to 6 carbon atoms, or aryl;

each R1 is independently hydrogen or methyl; and

each Q1 is independently —O—, —S—, or —N(R″)—, wherein R″ is hydrogen or alkyl having up to 6 carbon atoms.

In a second embodiment, the present disclosure provides the method according to the first embodiment, wherein the solvent comprises at least one of water, a monohydroxy alcohol, an ether, a ketone, a glycol, a glycol ether, or supercritical carbon dioxide.

In a third embodiment, the present disclosure provides the method according to the first or second embodiment, wherein the fluorinated amphoteric compound is adsorbed on the hydrocarbon-bearing formation.

In a fourth embodiment, the present disclosure provides the method according to any one of the first to third embodiments, wherein the hydrocarbon-bearing formation comprises limestone.

In a fifth embodiment, the present disclosure provides the method according to the fourth embodiment, wherein the hydrocarbon-bearing formation comprises at least 50 percent by weight limestone, based on the total weight of the hydrocarbon-bearing formation.

In a sixth embodiment, the present disclosure provides the method according to any one of the first to fifth embodiments, wherein the fluorinated amphoteric compound is represented by formula:


wherein Rf is perfluoroalkyl having up to 6 carbon atoms, wherein each W is independently alkylene having up to 4 carbon atoms, and wherein Y′ is —SO3M, or —CO2M.

In a seventh embodiment, the present disclosure provides the method according to any one of the first to fifth embodiments, wherein the fluorinated amphoteric compound is represented by formula Rf-Q-Z, wherein Rf is perfluoroalkyl having up to 6 carbon atoms, Q is —SO2—N(R′)—W— or alkylene having up to four carbon atoms, wherein R′ is hydrogen or alkyl having up to four carbon atoms, and wherein W is alkylene having up to 4 carbon atoms.

In an eighth embodiment, the present disclosure provides the method according to any one of the first to fifth embodiments, wherein the fluorinated amphoteric compound is the compound comprising:

    • the first divalent unit represented by


and

    • the second divalent unit represented by formula


wherein Rf1 is perfluoroalkyl having up to 6 carbon atoms; Q is —SO2—N(R′)—W— or alkylene having up to four carbon atoms, wherein R′ is hydrogen or alkyl having up to four carbon atoms, and wherein W and V are each independently alkylene having up to four carbon atoms.

In a ninth embodiment, the present disclosure provides the method according to any one of the first to fifth embodiments, wherein Rf is selected from the group consisting of:
Rfd—(O)r—CHF—(CF2)n—;
[Rfe—(O)t—C(L)H—CF2—O]m—W′—;
CF3CFH—O—(CF2)p—;
CF3—(O—CF2)z—; and
CF3—O—(CF2)3—O—CF2—;
wherein

    • Rfd and Rfe independently represent a partially or fully fluorinated alkyl group having from 1 to 10 carbon atoms and optionally interrupted with at least one oxygen atom;
    • L is selected from the group consisting of F and CF3;
    • W′ is selected from the group consisting of alkylene and arylene;
    • r is 0 or 1, wherein when r is 0, then Rfd is interrupted with at least one oxygen atom;
    • t is 0 or 1;
    • m is 1, 2, or 3;
    • n is 0 or 1;
    • each p is independently a number from 1 to 6; and
    • z is a number from 2 to 7.

In a tenth embodiment, the present disclosure provides the method of any one of the first to fifth embodiments, wherein Rf is C3F7O(CF(CF3)CF2O)xCF(CF3)—, C3F7O(CF2CF2CF2O)xCF2CF2—, CF3O(C2F4O)yCF2—, or CF3O(CF2O)x′(C2F4O)y′CF2—, wherein x has an average value in a range from 3 to 50, and wherein y, x′, and y′ have average values in a range from 6 to 50.

In an eleventh embodiment, the present disclosure provides the method according to any one of the first to tenth embodiments, wherein each R is independently alkyl having up to four carbon atoms.

In a twelfth embodiment, the present disclosure provides the method according to any one of the first to eleventh embodiments, wherein Q is —SO2—N(R′)—W—.

In a thirteenth embodiment, the present disclosure provides the method according to any one of the first to twelfth embodiments, wherein the fluorinated amphoteric compound is present in the treatment composition in at up to 1 weight percent, based on the total weight of the treatment composition.

In a fourteenth embodiment, the present disclosure provides the method according to any one of the first to thirteenth embodiments, further comprising:

receiving data comprising a temperature and a brine composition of the hydrocarbon-bearing formation; and

selecting the treatment composition for treating the hydrocarbon-bearing formation, wherein, at the temperature, a mixture of an amount of the brine composition and the treatment composition is transparent and free of precipitated solid, and wherein the mixture does not separate into layers.

In a fifteenth embodiment, the present disclosure provides the method according to any one of the first to thirteenth embodiments, further comprising:

receiving data comprising a temperature and a brine composition of the hydrocarbon-bearing formation; and

selecting the treatment composition for treating the hydrocarbon-bearing formation, wherein, at the temperature, a mixture of the brine composition and the treatment composition separates into at least two separate transparent liquid layers, and wherein the mixture is free of precipitated solid.

In a sixteenth embodiment, the present disclosure provides the method according to any one of the first to thirteenth embodiments, further comprising:

receiving data comprising a temperature and a first brine composition of the hydrocarbon-bearing formation;

contacting the hydrocarbon-bearing formation with a fluid, wherein after the fluid contacts the hydrocarbon-bearing formation, the hydrocarbon-bearing formation has a second brine composition that is different from the first brine composition; and

selecting the treatment composition for treating the hydrocarbon-bearing formation, wherein, at the temperature, a mixture of an amount of the second brine composition and the treatment composition is transparent and free of precipitated solid, and wherein the mixture does not separate into layers.

In a seventeenth embodiment, the present disclosure provides the method according to any one of the first to sixteenth embodiments, wherein the hydrocarbon-bearing formation is a gas producing formation penetrated by a wellbore, and wherein a region near the wellbore is contacted with the treatment composition.

In an eighteenth embodiment, the present disclosure provides the method according to the seventeenth embodiment, further comprising obtaining gas from the wellbore after contacting the hydrocarbon-bearing formation with the treatment composition.

In a nineteenth embodiment, the present disclosure provides the method according to any one of the first to eighteenth embodiments, further comprising fracturing the hydrocarbon-bearing formation, wherein contacting the hydrocarbon-bearing formation with the treatment composition is carried out during the fracturing, after the fracturing, or during and after the fracturing.

In a twentieth embodiment, the present disclosure provides the method according to any one of the first to nineteenth embodiments, wherein the hydrocarbon-bearing formation has at least one fracture, and wherein the fracture has a plurality of proppants therein.

In a twenty-first embodiment, the present disclosure provides the method according to any one of the first to eighteenth embodiments, wherein the method does not include intentionally fracturing the hydrocarbon-bearing formation.

In a twenty-second embodiment, the present disclosure provides the method according to any one of the first to twenty-first embodiments, wherein before contacting the hydrocarbon-bearing formation with the treatment composition, the hydrocarbon-bearing formation has retrograde gas condensate, volatile oil, or black oil, and wherein the hydrocarbon-bearing formation has an increase in at least a gas permeability after it is contacted with the treatment composition.

In a twenty-third embodiment, the present disclosure provides a hydrocarbon-bearing formation treated according to the method of any one of the first to twenty-second embodiments.

Advantages and embodiments of the methods disclosed herein are further illustrated by the following examples, but the particular materials and amounts thereof recited in these examples, as well as other conditions and details, should not be construed to unduly limit this invention. Unless otherwise noted, all parts, percentages, ratios, etc. in the examples and the rest of the specification are by weight.

EXAMPLES

In the following Comparative Preparation A, a nonionic fluorinated polymeric surfactant (“Nonionic Fluorinated Polymeric Surfactant A”) was prepared according to the method of U.S. Pat. No. 6,664,354 (Savu), Example 2, Parts A and B, and Example 4, incorporated herein by reference, except using 4270 kilograms (kg) of N-methylperfluorobutanesulfonamidoethanol, 1.6 kg of phenothiazine, 2.7 kg of methoxyhydroquinone, 1590 kg of heptane, 1030 kg of acrylic acid, 89 kg of methanesulfonic acid (instead of triflic acid), and 7590 kg of water in the procedure of Example 2B and using 15.6 grams of 50/50 mineral spirits/TRIGONOX-21-C50 organic peroxide initiator (tert-butyl peroxy-2-ethylhexanoate obtained from Akzo Nobel, Arnhem, The Netherlands) in place of 2,2′-azobisisobutyronitrile, and with 9.9 grams of 1-methyl-2-pyrrolidinone added to the charges in the procedure of Example 4.

In the following Preparation 1, an intermediate C4F9SO2N(H)C3H6N(CH3)2 was prepared as described in U.S. Pat. No. 5,468,353 (Anich), column 7, lines 15-42, incorporated herein by reference.

In the following Preparation 2, an amphoteric compound C4F9SO2N(C2H4COOH)C3H6N(CH3)2 was prepared as described in U.S. Pat. No. 5,468,353 (Anich), column 7 lines 15-58, incorporated herein by reference.

In the following Preparations 3 and 4, N-methylperfluorobutanesulfonamide ethylmethacrylate (MeFBSEMA) was prepared as described in U.S. Pat. No. 6,664,354 (Savu) Example 2, Parts A and B, incorporated herein by reference, except with the modifications described above, and except that the acrylic acid was replaced with an equimolar amount of methacrylic acid.

Comparative Preparation A

The “Nonionic Fluorinated Polymeric Surfactant A” was combined as shown in Table 1, below, wherein the weight percentages were based upon the total weight percentage of the composition. The “Nonionic Fluorinated Polymeric Surfactant A” was added to a flask containing isopropyl alcohol and mixed together using a magnetic stirrer and a magnetic stir bar for 30 minutes. Propylene glycol was then added to the mixture and stirred for 15 minutes.

TABLE 1 “Nonionic Fluorinated Isopropyl Polymeric Surfactant alcohol Propylene Example A”. (%) (IPA) (%) Glycol (%) Comparative A 2.0 29.0 69.0

Preparation 1

In a three-necked flask of 250 ml fitted with a stirrer, thermometer, cooler and heating mantle, were placed 74 g (0.2 mol) of the compound C4F9SO2N(H)C3H6N(CH3)2, and 74 g of dimethylformamide (DMF) (available from Aldrich, Bornem, Belgium). The reaction was warmed up to 40° C. under nitrogen atmosphere.

Subsequently, 24.4 g (0.2 mol) of 1,3-propanesultone (available from Aldrich) was added and the temperature increased to 60° C. The reaction was carried out for 4 hours under nitrogen atmosphere.

20 g of the resulting amphoteric compound mixture was diluted to 1% by weight in with a solvent mixture comprising ethanol/water (80:20).

Preparation 2

C4F9SO2N(C2H4COOH)C3H6N(CH3)2 was diluted to 1% by weight in with a solvent mixture comprising ethanol/water (80:20).

Preparation 3

In a three-necked flask of 250 mL fitted with a stirrer, condenser and a thermometer, were placed 30 g (0.07 mol) of MeFBSEMA, 20 g (0.127 mol) of N,N-dimethylaminoethylmethacrylate (DMAEMA) (available from Aldrich), 2 g of 3-mercapto 1,2 propanediol (available from Aldrich), 50 g of DMF, and 0.1 g of azobisisobutyronitrile (AIBN) (available from Aldrich). The mixture was degassed 3 times under nitrogen and aspirator vacuum then heated to 75° C. under nitrogen atmosphere. After 4 hours of reaction, a second charge of initiator (0.05 g of AIBN) was added and the reaction was allowed to continue for 16 hours. The resulting clear reaction mixture was cooled to room temperature and 15.5 g of 1,3-propanesultone (0.127 mol) was added together with 15 g of DMF. An exothermic reaction resulted and the reaction continued for 3 hours at 60° C. under nitrogen atmosphere.

The reaction mixture was diluted to 1% by weight in with a solvent mixture of ethanol/water (82:18) by adding 4 g of the reaction mixture to a solvent mixture comprising 160 g of ethanol and 36 g of deionized water.

Preparation 4

Preparation 4 was prepared as described in Preparation 3, except that the reaction mixture was diluted to 0.75% with a solvent mixture of ethanol/water (80:20).

Preparation 5

In Preparation 5, an amphoteric fluorosurfactant (obtained from DuPont, Wilmington, USA under the trade designation “ZONYL FS-500”) was dissolved at 1% in a solvent mixture comprising ethanol/water (80:20).

Core Flood Set up and Procedure for Comparative Example A and Examples 1-4.

A schematic diagram of a flow apparatus 100 used to determine relative permeability of particulate calcium carbonate is shown in FIG. 2. Flow apparatus 100 included positive displacement pump 102 (Model Gamma/4-W 2001 PP, obtained from Prolingent AG, Regensdorf, Germany). Nitrogen gas was injected at constant rate through a gas flow controller 120 (Model DK37/MSE, Krohne, Duisburg, Germany). Pressure indicators 113, obtained from Siemens under the trade designation “SITRANS P” 0-16 bar, were used to measure the pressure drop across a particulate pack in vertical core holder 109 (20 cm by 12.5 cm2) (obtained from 3M Company, Antwerp, Belgium). A back-pressure regulator (Model No. BS(H)2; obtained from RHPS, The Netherlands) 104 was used to control the flowing pressure upstream and downstream of core holder 109. Core holder 109 was heated by circulating silicone oil, heated by a heating bath obtained from Lauda, Switzerland, Model R22.

The core holder was filled with particulate calcium carbonate (obtained Merck, Darmstadt, Germany as granular marble—0.5 to 2 mm size) and then heated to 75° C. A pressure of about 5 bar (5×105 Pa) was applied, and the back pressure was regulated in such a way that the flow of nitrogen gas through the particulate calcium carbonate was about 500 to 1000 mL/minute. The initial gas permeability was calculated using Darcy's law.

Synthetic brine, prepared according to the natural composition of North Sea brine, was prepared by mixing 5.9% sodium chloride, 1.6% calcium chloride, 0.23% magnesium chloride, and 0.05% potassium chloride and distilled water up to 100% by weight. The brine was introduced into the core holder at about 1 mL/minute using displacement pump 102.

Heptane was introduced at about 0.5 mL/minute into the core using displacement pump 102.

The fluorinated polymer composition (treatment composition) was then injected into the core at a flow rate of 1 mL/minute. The gas permeability after treatment was calculated from the steady state pressure drop, and improvement factor was calculated as the permeability after treatment/permeability before treatment.

After the treatment, heptane was introduced at about 0.5 mL/minute into the core using displacement pump 102.

Comparative Example A and Examples 1-5

For Comparative Example A, the core treatment was carried out using Comparative Preparation A. For Examples 1-5, Preparations 1-5 were used.

For all Examples, the liquid used, initial pressure (bar), the pressure change (ΔP), the flow rate for each injection, the amount of liquid used for each injection, the flow rate of gas through the core (Q), the gas permeability (K), and the improvement factor (PI) are shown in Table 2, below. In the table, the “-” means not measured or not applicable.

TABLE 2 Gas Initial Pressure Flow Amount Q Pressure change (mL/ Liquid (mL/ K Examples Liquid Injected (bar) (ΔP) min) (g) sec) (D) PI Comp. None (N2) 5.08 0.010 500 — 8.33 22.67 — Example Brine 5.23 0.138 450 42 7.95 1.57 — A Heptane 5.55 0.090 480 50 8.38 2.53 — Comp. Prep. A 5.87 0.063 480 45 8.24 3.55 1.40 Heptane 4.79 0.143 600 160 10.70 2.03 0.80 Example None (N2) 5.11 0.010 480 — 8.00 21.76 — 1 Brine 5.236 0.142 580 41 10.41 1.99 — Heptane 5.40 0.126 480 80 8.54 1.84 — Preparation 1 5.42 0.053 460 53 7.88 4.04 2.20 Heptane 5.52 0.067 450 150 7.70 3.13 1.70 Example None (N2) 5.07 0.010 550 — 9.17 24.96 — 2 Brine 5.22 0.014 520 43 9.27 1.76 — Heptane 5.39 0.134 500 60 8.91 1.81 — Preparation 2 5.55 0.060 520 40 8.92 4.04 2.23 Heptane 5.43 0.070 500 155 8.58 3.33 1.84 Example None (N2) 4.57 0.010 940 — 15.6 42.5 — 3 Brine 4.64 0.105 820 66 14.34 3.71 — Heptane 4.68 0.092 810 75 14.17 4.19 — Preparation 3 4.74 0.039 800 82 13.6 9.48 2.26 Heptane 4.78 0.046 800 229 13.63 8.06 1.92 Example None (N2) 3.84 0.01 950 — 15.8 43.0 — 4 Brine 4.02 0.095 490 82 8.54 2.44 — Heptane 4.03 0.090 460 89 8.01 2.42 — Preparation 4 4.03 0.034 370 90 6.34 5.03 2.07 Heptane 4.05 0.040 440 255 7.48 5.08 2.10 Example None (N2) 4.10 0.010 560 — 9.33 25.40 — 5 Brine 4.23 0.153 520 56 9.38 1.67 — Heptane 4.29 0.140 520 62 9.32 1.81 — Preparation 5 4.37 0.060 50 89 8.59 3.89 2.15 Heptane 4.37 0.072 530 210 9.16 3.46 1.91

The results of the evaluations using particulate calcium carbonate can be verified using core flood evaluations on limestone core samples. A schematic diagram of a core flood apparatus 200 that can be used is shown in FIG. 3. Core flood apparatus 200 includes positive displacement pump 202 (Model QX6000SS, obtained from Chandler Engineering, Tulsa, Okla.) to inject n-heptane at constant rate into fluid accumulators 216. Nitrogen gas can be injected at constant rate through a gas flow controller 220 (Model 5850 Mass Flow Controller, Brokks Instrument, Hatfield, Pa.). A pressure port 211 on high-pressure core holder 208 (Hassler-type Model RCHR-1.0 obtained from Temco, Inc., Tulsa, Okla.) can be used to measure pressure drop across the vertical core 209. A back-pressure regulator (Model No. BP-50; obtained from Temco, Tulsa, Okla.) 204 can be used to control the flowing pressure downstream of core 209. High-pressure core holder 208 can be heated with 3 heating bands 222 (Watlow Thinband Model STB4A2AFR-2, St. Louis, Mo.).

In a typical procedure, a core can be dried for 72 hours in a standard laboratory oven at 95° C. and then wrapped in aluminum foil and heat shrink tubing. Referring again to FIG. 3, the wrapped core 209 can placed in core holder 208 at the desired temperature. An overburden pressure of, for example, 2300 psig (1.6×107 Pa) can be applied. The initial single-phase gas permeability can be measured using nitrogen at low system pressures between 5 to 10 psig (3.4×104 to 6.9×104 Pa).

Deionized water or brine can be introduced into the core 209 by the following procedure to establish the desired water saturation. The outlet end of the core holder is connected to a vacuum pump and a full vacuum can be applied for 30 minutes with the inlet closed. The inlet can be connected to a burette with the water in it. The outlet is closed and the inlet is opened to allow 2.1 mL of water to flow into the core. The inlet and the outlet valves can then be closed for the desired time. The gas permeability can be measured at the water saturation by flowing nitrogen at 500 psig (3.4×106 Pa). The core holder 208 can then be heated to a higher temperature, if desired, for several hours. Nitrogen and n-heptane can be co-injected into the core at an average total flow rate in the core of, for example, 450 mL/hour at a system pressure of, for example, 900 psig (6.2×106 Pa) until steady state is reached. The flow rate of nitrogen is controlled by gas flow controller 220, and the rate for n-heptane is controlled by positive displacement pump 202. The flow rates of nitrogen and n-heptane can be set such that the fractional flow of gas in the core was 0.66. The gas relative permeability before treatment can then be calculated from the steady state pressure drop. The treatment composition can then be injected into the core at a flow rate of, for example, 120 mL/hour for about 20 pore volumes. Nitrogen and n-heptane co-injection can be resumed at an average total flow rate in the core of, for example, 450 mL/hour at a system pressure of, for example, 900 psig (6.2×106 Pa) until steady state is reached. The gas relative permeability after treatment can then be calculated from the steady state pressure drop.

Various modifications and alterations of this disclosure may be made by those skilled the art without departing from the scope and spirit of the disclosure, and it should be understood that this disclosure is not to be unduly limited to the illustrative embodiments set forth herein.

Claims

1. A method of treating a hydrocarbon-bearing formation, the method comprising: wherein

contacting the hydrocarbon-bearing formation with a treatment composition comprising solvent and a fluorinated amphoteric compound, wherein the hydrocarbon-bearing formation comprises carbonate, and wherein the fluorinated amphoteric compound is selected from the group consisting of: (a)
(b) Rf-Q-Z (c) a compound comprising: a first divalent unit represented by
and a second divalent unit represented by formula
and (d) combinations thereof;
Rf is independently fluoroalkyl having up to 10 carbon atoms or a polyfluoropolyether group;
each Rf1 is independently fluoroalkyl having up to 10 carbon atoms or a polyfluoropolyether group;
X is —SO2— or —C(O)—;
Y is —N(R)2, —+(R)3, or —N+(R)3A-, wherein A- is a counter anion;
Y′ is —P(O)(OM)2, —O—P(O)(OM)2, —SO3M, —O—SO3M, or —CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation;
each Q is independently —SO2—N(R′)—W—, —C(O)—N(R′)—W—, alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O—, —S—, —SO2— or —C(O)—;
each W is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl;
Z is —N+(R)2—V—SO3M, or —N+(R)2—V—CO2M, wherein M is hydrogen, a counter cation, a free anion, or a bond to the hydrocarbon-bearing formation;
each V is independently alkylene, arylalkylene, or arylene, wherein alkylene and arylalkylene are each optionally interrupted by —O— or —S— and optionally substituted by hydroxyl;
each R is independently hydrogen, alkyl, or aryl, wherein alkyl may optionally be interrupted by —O— or substituted with hydroxyl or aryl, or two R groups taken together with the N atom to which they are attached can form a heterocyclic ring having up to six carbon atoms and optionally containing —O— or —S—;
R′ is hydrogen, alkyl having up to 6 carbon atoms, or aryl;
each R1 is independently hydrogen or methyl; and
each Q1 is independently —O—, —S—, or —N(R″)—, wherein R″ is hydrogen or alkyl having up to 6 carbon atoms.

2. The method of claim 1, wherein the solvent comprises at least one of water, a monohydroxy alcohol, an ether, a ketone, a glycol, a glycol ether, or supercritical carbon dioxide.

3. The method according to claim 1, wherein the fluorinated amphoteric compound is represented by formula:

wherein Rf is perfluoroalkyl having up to 6 carbon atoms, wherein each W is independently alkylene having up to 4 carbon atoms, and wherein Y′ is —SO3M, or —CO2M.

4. The method according to claim 1, wherein the fluorinated amphoteric compound is represented by formula Rf-Q-Z, wherein Rf is perfluoroalkyl having up to 6 carbon atoms, Q is —SO2—N(R)—W— or alkylene having up to four carbon atoms, wherein R′ is hydrogen or alkyl having up to four carbon atoms, and wherein W is alkylene having up to 4 carbon atoms.

5. The method according to claim 1, wherein the fluorinated amphoteric compound is the compound comprising: and wherein Rf1 is perfluoroalkyl having up to 6 carbon atoms; Q is —SO2—N(R)—W— or alkylene having up to four carbon atoms, wherein R′ is hydrogen or alkyl having up to four carbon atoms, and wherein W and V are each independently alkylene having up to four carbon atoms.

the first divalent unit represented by
the second divalent unit represented by formula

6. The method according to claim 1, wherein Rf is selected from the group consisting of: wherein

Rfd—(O)r—CHF—(CF2)n—;
[Rfe—(O)t—C(L)H—CF2—O]m—W′—;
CF3CFH—O—(CF2)p—;
CF3—(O—CF2)z—;
and
CF3—O—(CF2)3—O—CF2—;
Rfd and Rfe independently represent a partially or fully fluorinated alkyl group having from 1 to 10 carbon atoms and optionally interrupted with at least one oxygen atom;
L is selected from the group consisting of F and CF3;
W′ is selected from the group consisting of alkylene and arylene;
r is 0 or 1, wherein when r is 0, then Rfd is interrupted with at least one oxygen atom;
t is 0 or 1;
m is 1, 2, or 3;
n is 0 or 1;
each p is independently a number from 1 to 6; and
z is a number from 2 to 7.

7. The method according to claim 1, wherein Rf is C3F7O(CF(CF3)CF2O)xCF(CF3)—, C3F7O(CF2CF2CF2O)xCF2CF2—, CF3O(C2F4O)yCF2—, or CF3O(CF2O)x′(C2F4O)y′CF2—, wherein x has an average value in a range from 3 to 50, and wherein y, x′, and y′ have average values in a range from 6 to 50.

8. The method according to claim 1, wherein each R is independently alkyl having up to four carbon atoms, and wherein Q is —SO2—N(R)—W—.

9. The method according to claim 1, wherein the fluorinated amphoteric compound is present in the treatment composition in at up to 1 weight percent, based on the total weight of the treatment composition.

10. The method according to claim 1, further comprising:

receiving data comprising a temperature and a brine composition of the hydrocarbon-bearing formation; and
selecting the treatment composition for treating the hydrocarbon-bearing formation, wherein, at the temperature, a mixture of an amount of the brine composition and the treatment composition is transparent and free of precipitated solid, and wherein the mixture does not separate into layers.

11. The method according to claim 1, further comprising:

receiving data comprising a temperature and a brine composition of the hydrocarbon-bearing formation; and
selecting the treatment composition for treating the hydrocarbon-bearing formation, wherein, at the temperature, a mixture of the brine composition and the treatment composition separates into at least two separate transparent liquid layers, and wherein the mixture is free of precipitated solid.

12. The method according to claim 1, further comprising:

receiving data comprising a temperature and a first brine composition of the hydrocarbon-bearing formation;
contacting the hydrocarbon-bearing formation with a fluid, wherein after the fluid contacts the hydrocarbon-bearing formation, the hydrocarbon-bearing formation has a second brine composition that is different from the first brine composition; and
selecting the treatment composition for treating the hydrocarbon-bearing formation, wherein, at the temperature, a mixture of an amount of the second brine composition and the treatment composition is transparent and free of precipitated solid, and wherein the mixture does not separate into layers.

13. The method according to claim 1, further comprising fracturing the hydrocarbon-bearing formation, wherein contacting the hydrocarbon-bearing formation with the treatment composition is carried out during the fracturing, after the fracturing, or during and after the fracturing.

14. The method according to claim 1, wherein the method does not include intentionally fracturing the hydrocarbon-bearing formation.

15. A hydrocarbon-bearing formation treated according to the method of claim 1.

16. The method according to claim 1, wherein the hydrocarbon-bearing formation comprises limestone.

17. The method according to claim 16, wherein the hydrocarbon-bearing formation comprises at least 50 percent by weight limestone, based on the total weight of the hydrocarbon-bearing formation.

18. The method according to claim 1, wherein the hydrocarbon-bearing formation has at least one fracture, and wherein the fracture has a plurality of proppants therein.

19. The method according to claim 1, wherein the hydrocarbon-bearing formation is a gas producing formation penetrated by a wellbore, and wherein a region near the wellbore is contacted with the treatment composition.

20. The method according to claim 1, wherein before contacting the hydrocarbon-bearing formation with the treatment composition, the hydrocarbon-bearing formation has retrograde gas condensate, volatile oil, or black oil, and wherein the hydrocarbon-bearing formation has an increase in at least a gas permeability after it is contacted with the treatment composition.

Referenced Cited
U.S. Patent Documents
2803615 August 1957 Ahlbrecht
3311167 March 1967 O'Brien
3394758 July 1968 Terry
3555100 January 1971 Garth
3653442 April 1972 Ross
3839425 October 1974 Bartlett
3902557 September 1975 Shaughnessy
4018689 April 19, 1977 Thompson
4200154 April 29, 1980 Tate
4329236 May 11, 1982 Alford
4432882 February 21, 1984 Raynolds et al.
4440653 April 3, 1984 Briscoe et al.
4460791 July 17, 1984 Cooke
4557837 December 10, 1985 Clark, III et al.
4565639 January 21, 1986 Penny
4594200 June 10, 1986 Penny
4609477 September 2, 1986 Crema
4702849 October 27, 1987 Penny
4753740 June 28, 1988 Marlett et al.
4767545 August 30, 1988 Karydas et al.
4817715 April 4, 1989 Peru
4823873 April 25, 1989 Karydas
4921619 May 1, 1990 Karydas
4923009 May 8, 1990 Watkins
4987254 January 22, 1991 Schwertfeger
4993448 February 19, 1991 Karydas et al.
4997580 March 5, 1991 Karydas et al.
5042580 August 27, 1991 Cullick
5092405 March 3, 1992 Prukop
5129457 July 14, 1992 Sydansk
5144069 September 1, 1992 Stern
5186257 February 16, 1993 Stahl et al.
5247993 September 28, 1993 Sarem et al.
5310002 May 10, 1994 Blauch et al.
5350497 September 27, 1994 Hung
5358052 October 25, 1994 Gidley
5468353 November 21, 1995 Anich et al.
5852148 December 22, 1998 Behr
6165948 December 26, 2000 Dewenter et al.
6182759 February 6, 2001 Burger
6206102 March 27, 2001 Pusch
6225263 May 1, 2001 Collins et al.
6255536 July 3, 2001 Worm
6380149 April 30, 2002 Flynn
6579572 June 17, 2003 Espin
6660693 December 9, 2003 Miller et al.
6664354 December 16, 2003 Savu et al.
6689854 February 10, 2004 Fan et al.
6729409 May 4, 2004 Gupta et al.
6770601 August 3, 2004 Brookey
6911417 June 28, 2005 Chan et al.
6945327 September 20, 2005 Ely et al.
6972274 December 6, 2005 Slikta et al.
7084094 August 1, 2006 Gunn et al.
7165613 January 23, 2007 Chan et al.
7417099 August 26, 2008 Savu et al.
7585817 September 8, 2009 Pope et al.
7629298 December 8, 2009 Arco et al.
7678426 March 16, 2010 Flynn
7772162 August 10, 2010 Pope et al.
7855169 December 21, 2010 Pope et al.
8043998 October 25, 2011 Pope et al.
8138127 March 20, 2012 Pope
8176981 May 15, 2012 Savu
8236737 August 7, 2012 Fan
8261825 September 11, 2012 Pope et al.
8403050 March 26, 2013 Pope et al.
8418759 April 16, 2013 Moore
20020023752 February 28, 2002 Qu
20030092581 May 15, 2003 Crews
20050054804 March 10, 2005 Dams
20050244641 November 3, 2005 Vincent
20060045979 March 2, 2006 Dams
20060148671 July 6, 2006 Dams
20060149012 July 6, 2006 Terrazas
20070015864 January 18, 2007 Hintzer
20070029085 February 8, 2007 Panga et al.
20070221877 September 27, 2007 Audenaert
20070225176 September 27, 2007 Pope
20070243389 October 18, 2007 Audenaert
20080008891 January 10, 2008 Dams
20080176771 July 24, 2008 Reddy et al.
20090281002 November 12, 2009 Casper
20100152071 June 17, 2010 Pope et al.
20100179262 July 15, 2010 Dams
20100181068 July 22, 2010 Pope et al.
20100224361 September 9, 2010 Pope
20100270019 October 28, 2010 Pope et al.
20100270020 October 28, 2010 Baran, Jr.
20100270021 October 28, 2010 Baran, Jr.
20100276142 November 4, 2010 Skildum et al.
20100288498 November 18, 2010 Moore et al.
20110056689 March 10, 2011 Baran, Jr.
20110124532 May 26, 2011 Maurer
20110136704 June 9, 2011 Sharma
20110177983 July 21, 2011 Baran, Jr.
20110201531 August 18, 2011 Sharma
20110232530 September 29, 2011 Dams
20110247822 October 13, 2011 Dams
20110247823 October 13, 2011 Dams
20120071372 March 22, 2012 Iaconelli
20130264061 October 10, 2013 Baran, Jr.
20130269932 October 17, 2013 Dams
20140014330 January 16, 2014 Dams
Foreign Patent Documents
2009732 August 1990 CA
2031482 April 1980 GB
2245622 January 1992 GB
1706204 November 1994 SU
WO 03/089540 October 2003 WO
WO 2005/028589 March 2005 WO
WO 2005/035936 April 2005 WO
WO 2007-017806 February 2007 WO
WO 2007/017806 February 2007 WO
WO 2007/033489 March 2007 WO
WO 2007/097975 August 2007 WO
WO 2008-118242 October 2008 WO
WO 2008-154245 December 2008 WO
Other references
  • Adibhatla, “Effect of Surfactants on Wettability of Near-wellbore Regions of Gas Reservoirs”, Journal of Petroleum Science and Engineering, 2006, vol. 52, pp. 227-236. (XP002519991).
  • Al-Anazi et al., “A Successful Methanol Treatment in a Gas-Condensate Reservoir: Field Application”, Mar. 2003, SPE 80901, Society of Petroleum Engineers Inc., pp. 1-9.
  • Al-Hamadah, “Handling Tight Gas/Condensate Carbonates: A Simulation Approach”, International Petroleum Technology Conference, Nov. 21-23 2005, pp. 1-7, SPE paper IPTC 10033.
  • Clark, H. B., et al., “Use of Fluorochemical Surfactants in Nonaqueous Stimulation Fields,” Journal of Petroleum Chemistry vol. 32, No. 10 (1980) p. 1695-1697.
  • Crema et al., “Foaming of Anhydrous Methanol for Well Stimulation”, Apr. 1985, SPE 13565, Society of Petroleum Engineers Inc., 4 pages.
  • DuPont™ Zonyl® Fluorosurfactants, Well Stimulation Additives brochure, 2006, 2 pages.
  • Fahes, “Wettability Alteration to Intermediate Gas-Wetting in Gas-Condensate Reservoirs at High Temperatures”, Oct. 9-12, 2005, SPE Annual Technical Conference and Exhibition, Dallas, TX, pp. 1-14. SPE 96184.
  • Kamath, “Laboratory Based Evaluation of Gas Well Deliverability Loss Due to Waterblocking”, Oct. 1-4, 2000, SPE Annual Technical Conference and Exhibition, Dallas, TX, pp. 605-619. SPE 63161.
  • Kumar, “Chemical Stimulation of Gas/Condensate Reservoirs”, Sep. 24-27, 2006, SPE Annual Technical Conference and Exhibition, San Antonio, TX, vol. 4, pp. 2688-2696. SPE 102669.
  • Kumar, “Improving the Gas and Condensate Relative Permeability Using Chemical Treatments”, May 15-17, 2006, SPE Gas Technology Symposium, Calgary, Alberta, pp. 1-9. SPE 100529.
  • Li, K. et al., “Experimental Study of Wettability Alteration to Preferential Gas-Wetting in Porous Media and Its Effects”, SPE Reservoir Eval. and Eng 3 (2), pp. 139-149.
  • Mahadevan, “Capillary Wicking in Gas Wells”, SPE Journal, Dec. 2007, pp. 429-437, SPE 103229.
  • Mahadevan, “Clean-up of Water Blocks in Low Permeability Formations”, Oct. 5-8, 2003, SPE Annual Technical Conference and Exhibition, Denver, Colorado, pp. 1-8, SPE 84216.
  • Mahadevan, “Evaporative Clean-up of Water-Blocks in Gas Wells”, Apr. 17-19, 2005, SPE Production and Operations Symposium, Oklahoma City, OK, pp. 1-11, SPE 94215.
  • McLeod, “The Use of Alcohol in Gas Well Stimulation”, Nov. 10-11, 1966, SPE Eastern Regional Meeting, Columbus, Ohio, pp. 1-13, SPE 1663.
  • Noh et al., “Experimental Study of Wettability Alteration for Reservoir Rock”, Project 3-Gas Condensate Reservoirs Part 2, Reservoir Engineering Research Institute, Apr. 1-Jun. 30, 2Q.05.
  • Noh et al., “Effect of Wettability on High-Velocity Coefficient in Two-Phase Gas-Liquid Flow”, SPE 102773, 2006 SPE Annual Technical Conference and Exhibition held in San Antonio, TX, Sep. 24-27, 2006.
  • Panga, “Preventive Treatment for Enhancing Water Removal From Gas Reservoirs by Wettability Alteration”, Mar. 11-14, 2007, 15th Middle East Oil & Gas Show and Conference, Kingdom of Bahrain, pp. 1-12, SPE 105367.
  • Tang, “Relative Permeability Modification in Gas/Liquid Systems Through Wettability Alteration to Intermediate Gas Wetting”, SPE Reservoir Evaluation & Engineering, Dec. 2002, vol. 5, No. 6, pp. 427-436. SPE 81195.
  • Tiab, “Petrophysics : Reservoir Rock Properties”, Second Edition, Theory and Practice of Measuring Reservoir Rock and Fluid Transport Properties, 2004, p. 426 , p. 382 , pp. 367-370.
  • Vikingstad, “Effect of surfactant structure on foam-oil interactions Comparing fluorinated surfactant and alpha elefin sulfonate in static foam tests”, Colloids and Surfaces A: Physicochem. Eng. Aspects, 2006, vol. 279, pp. 105-112.
  • ISA 210 International Search Report for PCT/US2010/040870, mailed on Feb. 23, 2011, 5 pages.
Patent History
Patent number: 8833449
Type: Grant
Filed: Jul 2, 2010
Date of Patent: Sep 16, 2014
Patent Publication Number: 20120097393
Assignee: 3M Innovative Properties Company (St. Paul, MN)
Inventors: Rudolf J. Dams (Antwerp), Steven J. Martin (Shoreview, MN), Yong K. Wu (Woodbury, MN)
Primary Examiner: Zakiya W Bates
Application Number: 13/382,554
Classifications
Current U.S. Class: Material Placed In Pores Of Formation To Treat Resident Fluid Flowing Into Well (166/279); Fracturing Characteristic (166/250.1); Chemical Inter-reaction Of Two Or More Introduced Materials (e.g., Selective Plugging Or Surfactant) (166/300); Placing Fluid Into The Formation (166/305.1); Using A Chemical (epo) (166/308.2)
International Classification: E21B 43/22 (20060101); E21B 43/26 (20060101); C09K 8/60 (20060101); B01F 17/00 (20060101); C08F 8/44 (20060101); C03C 12/02 (20060101); C09K 8/68 (20060101); C25C 1/00 (20060101);